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The main questions the study aims to answer are: |
* What are the mean and variance of the normal sound-induced vibration level at two anatomical locations, the umbo of the malleus and the tip of the incus? |
* Are there any significant differences in these vibrational responses associated with sex or age? |
Participants will have their ossicular mobility measured with an investigational medical device that sends light into the middle ear and measures the motion-induced phase shift on light reflected from the target structures when a sound stimulus is presented. Standard hearing tests including audiometry and tympanometry ... |
<|newrecord|> nctId: NCT06310265 id: TABED 1-24-21 briefTitle: Our Anesthesia Experiment Applied to Child Earthquake Victims in the February 6, 2023 Earthquake overallStatus: RECRUITING date: 2024-03-12 date: 2024-04-05 date: 2024-04-22 date: 2024-03-15 date: 2024-04-19 name: Ankara City Hospital Bilkent class: OTHER b... |
<|newrecord|> nctId: NCT06310252 id: PRO_010-2023 briefTitle: Safety and Efficacy of an Intrastromal Transform Corneal Allograft (TCA) for Presbyopia Correction - Long Term Follow-up overallStatus: RECRUITING date: 2024-02-13 date: 2024-06 date: 2024-09 date: 2024-03-15 date: 2024-03-15 name: Allotex, Inc. class: INDUS... |
A maximum of 101 eyes of qualified and consented subjects will undergo long term follow-up after instrastromal implantation of the TCA for presbyopia. conditions: Presbyopia studyType: OBSERVATIONAL observationalModel: COHORT timePerspective: PROSPECTIVE count: 101 type: ESTIMATED name: Opthalmic assessments measure: A... |
<|newrecord|> nctId: NCT06310239 id: WRNMMC-2023-0434 id: 67407 type: OTHER_GRANT domain: PRORP briefTitle: Microbiome Population Adaptation Study acronym: OLIMPAS overallStatus: RECRUITING date: 2023-12-01 date: 2027-11-30 date: 2029-11-30 date: 2024-03-15 date: 2024-03-15 name: Walter Reed National Military Medical C... |
<|newrecord|> nctId: NCT06310226 id: 23-000347 briefTitle: Phenotyping Response to Spinal Cord Stimulation in Chronic Low Back Pain overallStatus: RECRUITING date: 2024-04-01 date: 2025-03-01 date: 2025-03-01 date: 2024-03-15 date: 2024-03-15 name: University of California, Los Angeles class: OTHER briefSummary: Chroni... |
<|newrecord|> nctId: NCT06310213 id: 17368 briefTitle: Non-Invasive Pressure Monitor for Neonates & Infants at Risk of Developing Hydrocephalus overallStatus: NOT_YET_RECRUITING date: 2024-04-01 date: 2028-06-01 date: 2028-07-01 date: 2024-03-15 date: 2024-03-15 name: Indiana University class: OTHER briefSummary: The g... |
* Can the device distinguish between intracranial pressure variations in neonates and infants diagnosed with hydrocephalus and those without |
* Can the device compare pressure dynamics between pre- and post-operative periods in neonates and infants who undergo surgical treatments Participants will undergo standard of care evaluations for hydrocephalus (anterior fontanelle assessment and head circumference measurement) and wear the device during standard of c... |
<|newrecord|> nctId: NCT06310200 id: IRB-2023-398 briefTitle: Sphenopalatine Ganglion Block and Cold Induced Headaches overallStatus: NOT_YET_RECRUITING date: 2024-04-01 date: 2024-06-01 date: 2024-07-01 date: 2024-03-15 date: 2024-03-15 name: Wright State University class: OTHER briefSummary: The primary objective of ... |
<|newrecord|> nctId: NCT06310187 id: STUDY00023967 id: U54DA058271-01 type: NIH link: https://reporter.nih.gov/quickSearch/U54DA058271-01 briefTitle: Little Cigar Oxidants overallStatus: NOT_YET_RECRUITING date: 2024-07 date: 2029-08 date: 2029-08 date: 2024-03-15 date: 2024-03-15 name: Milton S. Hershey Medical Center... |
<|newrecord|> nctId: NCT06310174 id: IRB00362883 briefTitle: Study Examining the Effect of a Novel Cannulation Knife on User Satisfaction and Common Central Venous Catheter Insertion Complications acronym: SCAD overallStatus: RECRUITING date: 2023-12-22 date: 2026-03 date: 2027-05 date: 2024-03-15 date: 2024-03-15 name... |
<|newrecord|> nctId: NCT06310161 id: 855161 briefTitle: Light Therapy in End Stage Kidney Disease overallStatus: NOT_YET_RECRUITING date: 2024-08-01 date: 2024-12-01 date: 2025-03-01 date: 2024-03-15 date: 2024-04-23 name: University of Pennsylvania class: OTHER briefSummary: The goal of this clinical trial is to test ... |
<|newrecord|> nctId: NCT06310148 id: UW 24-019 briefTitle: Evaluation of the Chronic Disease Co-Care Pilot Scheme overallStatus: RECRUITING date: 2024-01-18 date: 2025-07-01 date: 2026-12-31 date: 2024-03-15 date: 2024-03-22 name: The University of Hong Kong class: OTHER name: Health and Medical Research Fund name: Pri... |
This is a 12-month cohort study among the District Health Centre (DHC) or DHC Express, healthcare providers, CDCC participants and a comparison group of 1,886 non-participants. All the person-in charge, 2 family doctors and 1 of each allied health provider from each DHC/DHC Express will be administered with the questio... |
Participant characteristics, enablement, compliance to the standards of care, and costing of CDCC Pilot Scheme will be summarized using descriptive statistics. Differences in the proportion of patients meeting treatment targeted for HT, pre-DM and DM after 12 months will be compared by chi-squared test and logistic reg... |
<|newrecord|> nctId: NCT06310135 id: STUDY-23-00816 briefTitle: Filtered Eyewear to Prevent Light-induced Melatonin Suppression - Aim 1 overallStatus: NOT_YET_RECRUITING date: 2024-05 date: 2025-05 date: 2025-05 date: 2024-03-15 date: 2024-03-15 name: Icahn School of Medicine at Mount Sinai class: OTHER briefSummary: T... |
<|newrecord|> nctId: NCT06310122 id: ESWT on planter fascitis briefTitle: Effect of Extracorporeal Shockwave Therapy on Gait Parameters in Patients With Planter Fascitis overallStatus: NOT_YET_RECRUITING date: 2024-03-12 date: 2024-09-01 date: 2025-03-30 date: 2024-03-15 date: 2024-03-15 name: Cairo University class: O... |
* to determine the effect of extracorporeal shockwave on pain intensity in patients with plantar fasciitis. |
* to determine the effect of extracorporeal shockwave on foot function in patients with plantar fasciitis. |
* to determine the effect of extracorporeal shockwave on gait parameters in patients with plantar fasciitis conditions: Plantar Fascitis conditions: Extracorporeal Shockwave Therapy studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL interventionModelDescription: Two groups : group (... |
<|newrecord|> nctId: NCT06310109 id: 2358_OPBG 2020 briefTitle: Effect of Pediatric Intensive Care Unit Diaries on PICS-p acronym: PICS-p overallStatus: RECRUITING date: 2021-07-14 date: 2024-05-31 date: 2024-10-31 date: 2024-03-15 date: 2024-03-15 name: Bambino Gesù Children's Hospital IRCCS class: OTHER name: Ministr... |
To help understand and improve these experiences, the investigators want to study the "PICU diaries." These are journals that families and hospital staff can write in during the child's time in the hospital. Parents, other visitors and healthcare professionals can share thoughts, experiences, and even drawings or photo... |
The investigators believe that writing in these diaries might help children and their families feel better after leaving the hospital. It might help kids feel less worried or sad, and it might also help their parents or caregivers feel better too. |
The study will include children who have been in the PICU and their families. Some families will receive these special diaries to use during their time in the hospital, while others won't. We'll then see how everyone feels after they leave the hospital and compare the two groups to see if the diaries make a difference. |
The investigators hope that by understanding how these diaries can help, healthcare professionals can make hospital experiences better for everyone involved. conditions: Post Intensive Care Syndrome conditions: Narrative Medicine conditions: Post Traumatic Stress Disorder conditions: Anxiety conditions: Depression stud... |
<|newrecord|> nctId: NCT06310096 id: E-59394181-604.01-79277 briefTitle: Role of Thoracolumbar Fascia Stretching on Pain Parameters With Non-Specific Chronic Low Back Pain overallStatus: RECRUITING date: 2024-01-01 date: 2024-03-11 date: 2024-03-11 date: 2024-03-15 date: 2024-03-15 name: Atılım University class: OTHER ... |
<|newrecord|> nctId: NCT06310083 id: SMR for Turbinate Hypertrophy briefTitle: Endoscopic Submucosal Resection Turbinoplasty VS Turbinectomy overallStatus: COMPLETED date: 2023-02-01 date: 2024-01-31 date: 2024-01-31 date: 2024-03-15 date: 2024-03-15 name: Ahmed Nabil Selim class: OTHER briefSummary: The aim of our stu... |
Group A (study group): who applied for Endoscopic submucosal resection Turbinoplasty. |
Group B (control group): Who applied for partial inferior turbinectomy. primaryPurpose: TREATMENT masking: QUADRUPLE maskingDescription: The surgeons performed the nasal surgery and evaluating postoperative measurable outcomes was blinded about cases who were subjected to Endoscopic submucosal resection Turbinoplasty w... |
<|newrecord|> nctId: NCT06310070 id: IRB-23-1965 briefTitle: 3D Printed Personalized Ostomy Appliance acronym: 3DPPOA overallStatus: NOT_YET_RECRUITING date: 2025-03-05 date: 2025-03-05 date: 2025-06-05 date: 2024-03-13 date: 2024-03-21 name: Carilion Clinic class: OTHER name: Virginia Polytechnic Institute and State U... |
• Whether or not a 3D scan of a stoma reduces leakages and improves patient quality of life in regard to using a personalized ostomy appliance. |
Participants will |
* Spend 2 weeks with their standard of care ostomy appliance |
* Spend 2 weeks with their personalized ostomy appliance made from a 3D scan |
* Participate in daily surveys and weekly quality of life surveys conducted over the phone conditions: 3D Printing conditions: Ostomy conditions: Leakage studyType: INTERVENTIONAL phases: NA allocation: NA interventionModel: SINGLE_GROUP primaryPurpose: PREVENTION masking: NONE count: 30 type: ESTIMATED name: 3D Printe... |
<|newrecord|> nctId: NCT06310057 id: 4139 briefTitle: Tofacitinib in the Treatment of Refractory Axial Spondyloarthritis Patients: A Dose Escalation Study overallStatus: COMPLETED date: 2022-01-01 date: 2024-03-01 date: 2024-03-01 date: 2024-03-13 date: 2024-03-13 name: Bangabandhu Sheikh Mujib Medical University, Dhak... |
The main question\[s\] it aims to answer are: |
* Efficacy and safety of tofacitinib in different doses |
* If escalation of tofacitinib is justified if clinical criteria is not fulfilled at 10mg conditions: Axial Spondyloarthritis studyType: INTERVENTIONAL phases: PHASE4 allocation: NON_RANDOMIZED interventionModel: PARALLEL interventionModelDescription: Dose escalation study, all the patients will recieve 10mg tofacitini... |
<|newrecord|> nctId: NCT06310044 id: Commiphora Myrrh briefTitle: Effect of Commiphora Myrrh Solution as a Root Canal Irrigant on Post Operative Pain and Bacterial Load Reduction in Necrotic Tooth overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2025-01-01 date: 2025-01-01 date: 2024-03-13 date: 2024-03-13 name... |
<|newrecord|> nctId: NCT06310031 id: CL-00545 briefTitle: [Trial of device that is not approved or cleared by the U.S. FDA] overallStatus: WITHHELD date: 2024-03-13 date: 2024-03-13 name: [Redacted] hasResults: False |
<|newrecord|> nctId: NCT06310018 id: 2023A070902 briefTitle: Augmented Ultrasound-Facilitated, Catheter-Directed Fibrinolysis for PE acronym: SONIC-PE overallStatus: NOT_YET_RECRUITING date: 2024-06-30 date: 2025-06-30 date: 2025-12-31 date: 2024-03-13 date: 2024-03-15 name: Brigham and Women's Hospital class: OTHER na... |
<|newrecord|> nctId: NCT06310005 id: 1466-0003 briefTitle: A Study in Healthy Japanese Men to Test How Well Different Doses of BI 3006337 Are Tolerated overallStatus: RECRUITING date: 2024-04-01 date: 2024-10-18 date: 2024-10-18 date: 2024-03-13 date: 2024-04-09 name: Boehringer Ingelheim class: INDUSTRY briefSummary: ... |
<|newrecord|> nctId: NCT06309992 id: 1404-0056 id: 2023-505303-23-00 type: REGISTRY domain: CTIS id: U1111-1299-9925 type: REGISTRY domain: WHO registry briefTitle: A Study to Test Whether Survodutide Helps People Living With Obesity or Overweight and With a Confirmed or Presumed Liver Disease Called Non-alcoholic Stea... |
* presumed or confirmed NASH together with overweight or obesity and |
* a body mass index (BMI) of 30 kg/m² or more, or |
* a BMI of 27 kg/m² and at least one weight-related health problem. |
People with a history of other chronic liver diseases cannot take part in this study. |
The purpose of this study is to find out whether a medicine called survodutide helps people living with obesity or overweight and a confirmed or presumed liver disease called nonalcoholic steatohepatitis (NASH) to have less liver fat and to lose weight. Participants are put into 2 groups randomly, which means by chance... |
Participants are in the study for about 1 year and 3 months. During this time, it is planned that participants visit the study site up to 13 times and receive 3 phone calls by the site staff. The doctors check participants' health and take note of any unwanted effects. The participants' body weight is regularly measure... |
<|newrecord|> nctId: NCT06309979 id: 111-903 briefTitle: A Study to Assess Growth in Children With Idiopathic Short Stature overallStatus: RECRUITING date: 2024-03-25 date: 2040-12-31 date: 2040-12-31 date: 2024-03-13 date: 2024-03-13 name: BioMarin Pharmaceutical class: INDUSTRY briefSummary: Study 111-903 will genera... |
<|newrecord|> nctId: NCT06309966 id: BHV7000-303 id: 2023-808811-21-00 type: REGISTRY domain: EU CTR briefTitle: Study to Determine if BHV-7000 is Effective and Safe in Adults With Refractory Focal Onset Epilepsy acronym: RISE 3 overallStatus: RECRUITING date: 2024-04 date: 2025-08 date: 2025-09 date: 2024-03-13 date: ... |
<|newrecord|> nctId: NCT06309953 id: 937 briefTitle: A Study to Evaluate Early Treatment Outcomes With Miebo™ in Subjects With Dry Eye Disease overallStatus: RECRUITING date: 2024-02-28 date: 2024-06-28 date: 2024-06-28 date: 2024-03-13 date: 2024-03-15 name: Bausch & Lomb Incorporated class: INDUSTRY briefSummary: An ... |
<|newrecord|> nctId: NCT06309940 id: Basal ganglionic haemorrhage briefTitle: Prognostic Factors for Surgical Management of Large Hypertensive Basal Ganglionic Haemorrhage overallStatus: NOT_YET_RECRUITING date: 2024-03 date: 2025-03 date: 2025-04 date: 2024-03-13 date: 2024-03-13 name: Assiut University class: OTHER b... |
<|newrecord|> nctId: NCT06309927 id: 0025-24-ASF briefTitle: Operative Hysteroscopy Versus Suction Curettage for Surgical Termination of Early Pregnancy Loss (Miscarriage) overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2025-12 date: 2025-12 date: 2024-03-13 date: 2024-03-13 name: Assaf-Harofeh Medical Center cla... |
Qualifying patients will sign an informed consent form and will be randomly assigned to the two arms of the study: |
1. Surgical uterine evacuation by the traditional ultrasound-guided suction curettage (control group) |
2. Surgical uterine evacuation by operative hysteroscopy using a tissue removal device (study group). |
The surgical procedure will be determined randomly by computer generated allocation. |
All surgical procedures will be performed under general anesthesia in an outpatient surgical suite. The operative time, operative blood loss and intraoperative complications will be recorded by the research team. |
Following the surgical procedure, the patients will be monitored and discharged home as per our department's day-surgery protocol. Immediate post-operative complications will be recorded until discharge. |
One week after the procedure, a telephone interview will be conducted to assess any procedure-related complications. |
A diagnostic hysteroscopy without anesthesia will be scheduled 6 weeks postoperatively to assess for retained products of conception and for intrauterine adhesions. The diagnostic hysteroscopy will be performed by a practitioner who will be blinded to the type of surgery performed. |
6 months after the procedure, a telephone questionnaire will be conducted to assess for subsequent pregnancies. conditions: Early Pregnancy Loss conditions: Intrauterine Adhesion studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL primaryPurpose: TREATMENT masking: SINGLE whoMasked: ... |
<|newrecord|> nctId: NCT06309914 id: Pro00074459 briefTitle: The Effects of Mirtoselect®, Virtiva®, and Enovita® on Cognitive Performance and Mood States overallStatus: RECRUITING date: 2024-02-21 date: 2024-03-15 date: 2024-05-06 date: 2024-03-13 date: 2024-03-13 name: Applied Science & Performance Institute class: IN... |
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