Doula Model of Care
NCT06915259
Recruiting
The goal of this randomized controlled intervention trial is to determine if an integrated partnership between a birth worker/community support organization and the Hospital of the University of Pennsylvania (HUP), will improve both the experience and outcomes for Black birthing people. The main question it aims to answer is whether an integrated partnership between a birth worker/community support organization and the Hospital of the University of Pennsylvania (HUP) will mitigate bias and mist... Read More
Gender:
FEMALE
Ages:
Between 16 years and 55 years
Trial Updated:
04/20/2025
Locations: Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania
Conditions: Perinatal, Morbidity, Mental Health
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Fetoscopic Neural Tube Defect Repair
NCT06946563
Recruiting
This is a single-arm prospective study to record maternal and neonatal outcomes on subjects who undergo fetoscopic repair of Neural Tube Defects (NTD) at Oregon Health \& Science University (OHSU). Fetoscopic repair will take place between 24 weeks 0 days and 27 weeks 6 days gestation. Surgical, post-operative, delivery, and neonatal outcomes will be collected.
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
04/20/2025
Locations: Oregon Health & Science University, Portland, Oregon
Conditions: Neural Tube Defects, Spina Bifida
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Cryospray Therapy Versus Standard of Care for Benign Airway Stenosis (CryoStasis)
NCT04996173
Recruiting
Benign central airway stenosis (BCAS) is an important cause of both pulmonary morbidity and mortality. Notable causes include post-intubation stenosis, collagen vascular diseases, airway trauma, infectious and idiopathic subglottic stenosis (iSGS). Surgery is the preferred definite option; however, the first therapeutic attempt is usually endoscopic to temporarily restore airway patency and symptomatic improvement. Several endoscopic modalities exist for treatment. Most commonly, thermal or las... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
04/19/2025
Locations: University of Mississippi Medical Center, Jackson, Mississippi +2 locations
Conditions: Pulmonary Disease
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Impact of Bromocriptine on Clinical Outcomes for Peripartum Cardiomyopathy
NCT05180773
Recruiting
The study will enroll 200 women newly diagnosed with peripartum cardiomyopathy within 5 months postpartum in a randomized placebo controlled trial of bromocriptine therapy to evaluate its impact on myocardial recovery and clinical outcomes. Given that bromocriptine prevents breastfeeding, an additional 50 women with peripartum cardiomyopathy excluded from the trial due to a desire to continue breastfeeding but meeting all other entry criteria will be followed in an observational cohort.
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
04/19/2025
Locations: University of Alabama Birmingham, Birmingham, Alabama +63 locations
Conditions: Peripartum Cardiomyopathy, Postpartum
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Study of the Safety and Neuroprotective Capacity of Scp776 in Acute Ischemic Stroke
NCT05585606
Recruiting
A Randomized, Placebo-Controlled, Double-Blind, Multicenter Study of the Safety and Neuroprotective Capacity of Scp776 in Subjects Undergoing Endovascular Thrombectomy for Acute Ischemic Stroke
Gender:
ALL
Ages:
18 years and above
Trial Updated:
04/19/2025
Locations: HonorHealth Scottsdale Osborn Medical Center, Scottsdale, Arizona +13 locations
Conditions: Acute Ischemic Stroke (AIS)
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Evaluating the Safety and Tolerability of Orally Administered DF-003 in ROSAH Syndrome Patients
NCT06395285
Recruiting
The purpose of this study is to evaluate the safety and tolerability of DF-003 in retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and migraine headache (ROSAH) syndrome patients.
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
04/19/2025
Locations: National Institutes of Health Clinical Center, Bethesda, Maryland +3 locations
Conditions: ROSAH
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Management of Postoperative Discomfort in Young Children Following Dental Rehabilitation Under General Anesthesia
NCT06757075
Recruiting
The purpose of this study is to investigate the effectiveness of various oral analgesic regimens in minimizing post-operative pain and discomfort in young children following dental rehabilitation under general anesthesia (DRGA). In this randomized controlled trial, three analgesic regimens following DRGA in Franciscan Children's Hospital will be compared using both self-report and behavioral measures. The analgesic therapies to be investigated are ibuprofen monotherapy, alternating ibuprofen an... Read More
Gender:
ALL
Ages:
Between 4 years and 6 years
Trial Updated:
04/19/2025
Locations: Franciscan Children's Hospital, Brighton, Massachusetts
Conditions: Pain, Postoperative
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Behavioral Treatment of Insomnia in Active-Duty Service Members With Traumatic Brain Injury
NCT06867666
Recruiting
The objective of the study is to conduct a randomized controlled trial of Cognitive Behavioral Therapy for Insomnia (CBT-I) in a sample of active-duty sailors with a history of traumatic brain injury (TBI). The investigators will test the impact of CBT-I on insomnia symptoms as well as post-concussive symptoms, psychological symptoms, and neurocognitive functioning in comparison to treatment as usual. The investigators will also compare the effectiveness of traditional in-person CBT-I and CBT-I... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
04/19/2025
Locations: Naval Medical Center San Diego, San Diego, California
Conditions: Insomnia, TBI (Traumatic Brain Injury)
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Vaccine Confidence and Infodemic in Southeast Asia's Nusantara Sociocultural Sphere
NCT06947187
Recruiting
The goal of this clinical trial is to understand how well a culturally-specific "prebunking" video can improve vaccine information literacy and vaccine confidence among individuals in the Nusantara sociocultural sphere. The investigators hypothesize the individuals who watch the co-created "prebunking" intervention video will have improved vaccine literacy skills and vaccine confidence compared to individuals who watch a video about safe medication disposal.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
04/19/2025
Locations: University of California, Berkeley, Berkeley, California
Conditions: Misinformation
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University of Michigan "Nephrology Research BioBank"
NCT00381121
Recruiting
The purpose of the study is to create a Nephrology Tissue Biobank enabling the study of kidney disease from the perspectives of epidemiology, genetics and molecular biology.
Gender:
ALL
Ages:
All
Trial Updated:
04/18/2025
Locations: University of Michigan Health System, Ann Arbor, Michigan
Conditions: Chronic Kidney Disease
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Nephrotic Syndrome Study Network
NCT01209000
Recruiting
Minimal change disease (MCD), focal segmental glomerulosclerosis (FSGS), and Membranous nephropathy (MN), generate an enormous individual and societal financial burden, accounting for approximately 12% of prevalent end stage renal disease (ESRD) cases (2005) at an annual cost in the US of more than $3 billion. However, the clinical classification of these diseases is widely believed to be inadequate by the scientific community. Given the poor understanding of MCD/FSGS and MN biology, it is not s... Read More
Gender:
ALL
Ages:
80 years and below
Trial Updated:
04/18/2025
Locations: University of Southern California-Children's Hospital, Los Angeles, California +43 locations
Conditions: Minimal Change Disease (MCD), Membranous Nephropathy, Glomerulosclerosis, Focal Segmental
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Intra- and Inter-fraction Changes in Radiation Therapy
NCT02344121
Recruiting
Analysis to quantify intra-fraction, inter-fraction and post-treatment changes in tumor target volumes and surrounding normal organs in radiation therapy.
Gender:
ALL
Ages:
All
Trial Updated:
04/18/2025
Locations: Froedtert Hospital, Milwaukee, Wisconsin
Conditions: Cancer
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