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Found 410 ctsi-central-admin trials

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

Feasibility, Acceptability and Preliminary Effects of the Spiritual Care Assessment and Intervention (SCAI) Framework for Adults With Advanced Cancer and Their Caregivers (FCGs): A Clinical Pilot Trial

18 - 100
Accepts healthy volunteer
All genders
The purpose of this study is to test a spiritual care intervention for adults with advanced cancer and their caregivers.
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PROSPECTIVE MULTI-CENTER EVALUATION OF THE DURATION OF THERAPY FOR THROMBOSIS IN CHILDREN (the "Kids-DOTT" Trial)

20 or below
All genders
This study plans to learn more about the best type of treatment for children with blood clots in the veins.
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A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate Pembrolizumab Versus Placebo as Adjuvant Therapy Following Surgery and Radiation in Participants with High-risk Locally Advanced Cutaneous Squamous Cell Carcinoma(LA cSCC) (KEYNOTE-630).

18 - 100
All genders
The purpose of this study is to compare the recurrence-free survival (RFS), as assessed by the investigator and confirmed by biopsy, in individuals who receive pembrolizumab with individuals who receive placebo as adjuvant therapy.
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ACCL1633, The Effectiveness of Lactobacillus plantarum in Preventing Acute Graft-versus-Host Disease (GvHD) in Children undergoing Alternative Hematopoietic Progenitor Cell Transplantation (HCT)

2 - 25
All genders
The purpose of this study is to find out if the probiotic Lactobacillus plantarum (LBP) will prevent the development of GI aGvHD in children, adolescents, and young adults undergoing alternative alloHCT.
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Long-term Recovery in OUD

18 - 100
All genders
The goals of this project are: 1) Establish normative data on long-term recovery course of OUD across patients, community supports, and providers and 2) Quantify the impact of MAT on long-term recovery from OUD.
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Tocotrienol Against the Progression of End Stage Liver Disease

18 - 100
All genders
The purpose of this study is to see if oral tocotrienol (TCT) will significantly reduce the rise in Model for End Stage Liver Disease (MELD) score over time in patients with Nonalcoholic Steatohepatits (NASH).
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Effectiveness of two different forms of marine oil, derived from the New Zealand green lipped mussel (Perna canaliculus) and krill oil (Euphausia superba), on indirect markers of muscle damage and soreness during recovery from muscle damaging exercise in untrained men: a randomized controlled non-inferiority trial

18 - 30
Male
The purpose of this study is to evaluate the effects of PCSO-524®, and a blend of PCSO-524® (75%) and krill oil (25%) (ESPO-572®), on indirect markers of muscle damage, inflammation and soreness during recovery from muscle damaging exercise.
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A Phase 3, Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy and Open-Label Extension

7 - 100
Male
This study is being done to see if Ataluren will slow the progression of DMD in boys with DMD who have specific mutations.
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A Theoretically Informed mHealth Intervention to Improve Medication Adherence by Adults with Chronic Conditions: Technology Acceptance Model-Based Smartphone Medication Reminder App Training Session

40 - 100
All genders
As a potential way to support your medication taking and management, the aim of this study is to promote your smartphone medication reminder app use. To meet this aim, the purpose of this study is to provide you with a group session introducing a smartphone medication reminder app and to …
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The OVAL Study: A Randomized, Controlled, Double-Arm,Double-Blind, Multi-Center Study of Ofranergene Obadenovec (VB-111) Combined with Paclitaxel vs. Paclitaxel Combined with Placebo for the Treatment of Recurrent Platinum-Resistant Ovarian Cancer

18 - 100
Female
The purpose of this study is to compare the efficacy and safety of the experimental drug VB-111 in combination with the standard chemotherapy drug paclitaxel compared to using paclitaxel combined with placebo.
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