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Found 573 in-health trials

A listing of in-health medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

Post Market Evaluation of Clinical Safety and Performance of the Fitbone Transport and Lengthening System

B
Brian Mullis, MD
21 years or above
All genders
Observational
What is the purpose of this study?The goal of this observational study is to examine and confirm the clinical performance of the Fitbone Transport and Lengthening System in adult patients (21 years and older) who require lower-limb lengthening, fracture fixation and/or treatment for previous non-healing fracture. The main questions it aims …
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Attenuating DEPression with Internet CBT to Slow Cognitive Decline in Older ICU Survivors (ADEPT-ICU)

B
Babar Khan, MD
50 years - 100 years
All genders
Interventional
What is the purpose of this study?Depression affects one-third of intensive care unit (ICU) survivors and represents a potentially modifiable target to slow cognitive decline and reduce the risk of Alzheimer’s disease and related dementias (ADRD). Our multi-PI team proposes a two-arm RCT called ADEPT-ICU (Attenuating DEPression with Internet CBT …
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A post-market, prospective, multi-center, single-arm studyevaluating the safety and efficacy of the 3M V.A.C. Peel andPlace Dressing used in conjunction with 3M V.A.C.® Therapy

G
Greg Westin
22 years - 100 years
Accepts healthy volunteer
All genders
What is the purpose of this study?The purpose of this clinical study is to obtain post-market safety and efficacy data when the V.A.C.® Peel and Place dressing is used in conjunction with 3M™ V.A.C.® Therapy.THIS STUDY IS ENROLLING BY INVITATION ONLY
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Examination of the informed consent process as experienced by patients who have undergone a chemoembolization radioembolization or transjugular intrahepatic portosystemic shunt (TIPS) procedure

C
Claire Draucker
100 years or below
All genders
The purpose of this study is to describe the experiences of patients providing IC to undergo a de novo TIPS procedure.
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Effect of Early Weight Bearing on Rehabilitation Outcomes in Patients with Traumatic Ankle and Tibial Plateau Fractures

R
Roman Natoli, MD
18 years - 65 years
All genders
The purpose of this study is to compare the usual practice of bearing weight (“delayed weight bearing”) with weight bearing sooner in the healing process. We will use study data to determine if early weight bearing improves recovery after injury.
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An Evaluation of Pediatric Neurodevelopmental Telehealth Services During COVID-19

R
Rebecca McNally Keehn
18 years - 100 years
All genders
The purpose of this study is to understand which families choose to receive telehealth services for their child with neurodevelopmental disability.
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CLARIFY: ADH1 and ADH2 Disease Monitoring Study (DMS)

E
Erik Imel, MD
90 years or below
All genders
Observational
A global, multi-center, Disease Monitoring Study (DMS) in participants with Autosomal Dominant Hypocalcemia Type 1 (ADH1) or Autosomal Dominant Hypocalcemia Type 2 (ADH2) designedharacterize ADH1 and ADH2 disease presentation and progression through retrospective (past) and longitudinal prospective (over time into the future) data collection.
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Evaluation of a New Strategy for Protocolized Antibiotic Care for Severe Open Fractures: SEXTANT

K
Karl Shively
L
Luke A. Lopas, MD
18 years - 64 years
All genders
Phase 3
Interventional
The proposed study is a multi-center, prospective randomized controlled trial comparingurrent standard of care treatment to the SEXTANT treatment protocol in patients with Typeures of the tibia and IIIB fractures of the ankle and hindfoot.
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Enasidenib for the Treatment of Relapsed or Refractory Acute Myeloid Leukemia Patients With an IDH2 Mutation

S
Sandeep Batra, MD
24 months - 18 years
All genders
Phase 2
Interventional
What is the purpose of this study?This trial studies the side effects of enasidenib and to see how well it works in treatingwith acute myeloid leukemia that has come back after treatment (relapsed) or has been difficult to treat with chemotherapy (refractory). Patients must also have a specific genetic change, …
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Evaluation of VX-121/Tezacaftor/Deutivacaftor in Cystic Fibrosis (CF) Participants 1 Through 11 Years of Age

J
James Chmiel
1 year - 11 years
All genders
Phase 3
Interventional
The purpose of this study is to evaluate the pharmacokinetics, safety, tolerability andy of VX-121/tezacaftor/deutivacaftor (VX-121/TEZ/D-IVA) in CF participants with at1 triple combination responsive (TCR) mutation in the cystic fibrosis transmembraneductance regulator (CFTR) gene.
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