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NCT ID: NCT04774965 Not yet recruiting - Surgery Clinical Trials

The Effects of SlumberCurve™ Following Rotator Cuff Surgery: A Randomized Control Trial

Start date: June 30, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effects of a novel sleep aid known as SlumberCurve™, which serves as an adjustable form of a wedge pillow, on sleep quality and pain management following rotator cuff repair. The researchers hypothesize that SlumberCurve™ will significantly improve sleep quality and reduce night-time pain.

NCT ID: NCT04774536 Not yet recruiting - Sickle Cell Disease Clinical Trials

Transplantation of Clustered Regularly Interspaced Short Palindromic Repeats Modified Hematopoietic Progenitor Stem Cells (CRISPR_SCD001) in Patients With Severe Sickle Cell Disease

Start date: June 1, 2024
Phase: Phase 1/Phase 2
Study type: Interventional

This is an open label, non-randomized, 2-center, phase 1/2 trial of a single infusion of sickle allele modified cluster of differentiation (CD34+) hematopoietic stem progenitor cells (HSPCs) in subjects with in subjects ≥12 years old to 35 years old severe Sickle Cell Disease (SCD). The study will evaluate the hematopoietic stem cell transplantation (HSCT) using CRISPR/Cas9 edited red blood cells (known as CRISPR_SCD001 Drug Product).

NCT ID: NCT04773340 Not yet recruiting - Clinical trials for Antisocial Personality Disorder

Adapting Dialectical Behavior Therapy for the Treatment of Criminal Offenders With Antisocial Personality Disorder

DBT-ASPD
Start date: October 1, 2021
Phase:
Study type: Observational

This pilot study is intended to adapt and refine an intervention grounded in the principles of Dialectical Behavior Therapy, for the treatment of repeat criminal offenders with antisocial personality disorder. This study will be open to individuals participating in an intensive supervision program operated by the U.S. District Court of the Southern District of New York (the RISE Court program).

NCT ID: NCT04771689 Not yet recruiting - Post-operative Pain Clinical Trials

Buprenorphine/Naloxone Micro-Dosing for Postoperative Pain Management in Opioid-Tolerant Patients

Start date: July 1, 2022
Phase: Phase 4
Study type: Interventional

A randomized clinical study evaluating the effect of buprenorphine/naloxone (bup/nx) sublingual film on postoperative pain management in opioid-tolerant patients.

NCT ID: NCT04770961 Not yet recruiting - Clinical trials for Mitral Regurgitation

Erector Spinae Plane Block for Minimally Invasive Mitral Valve Surgery

Start date: April 1, 2021
Phase: N/A
Study type: Interventional

The goal of this project is to study whether local anesthetic via the erector spinae plane (ESP) block may be beneficial in minimally invasive mitral valve surgery (MIMVS).

NCT ID: NCT04769336 Not yet recruiting - Laboratory Problem Clinical Trials

Effectiveness of Point of Care Complete Blood Cell Count Analyzer in Reducing Time to Results

Start date: April 1, 2021
Phase:
Study type: Observational

The current process for getting complete blood cell counts (CBC) results in the operating room during surgery relies on sending blood samples from the operating room to the hospital's central lab. This workflow is complex and often results in handing off the blood sample to 4 or more different staff members before arriving in the lab for analysis. This often causes delayed CBC results, which may lead to inappropriate or delayed clinical decision making. By providing prompt access to CBC results with the use of a point of care CBC analyzer, the clinical workflow efficiency can be significantly improved. This should resulting in better clinical decision making, reductions in costs, increase in patient satisfaction and facilitation of hospital processes.

NCT ID: NCT04768777 Not yet recruiting - Clinical trials for Multiple Sclerosis, Relapsing-Remitting

Behavioral Intervention for Physical Activity and Sexual Dysfunction in Multiple Sclerosis

BIPAMS-SD
Start date: December 1, 2024
Phase: N/A
Study type: Interventional

The prevalence of sexual dysfunction is higher among women with multiple sclerosis (MS) than women in the general population. The presence of sexual dysfunction is associated with decreased well-being and quality of life. There is limited research supporting pharmacological and other therapeutic approaches for managing sexual dysfunction in MS. Physical activity has beneficial effects on many of the consequences of MS, and physical activity represents a promising non-pharmacological approach for managing symptoms of sexual dysfunction in MS. The proposed research examines the effect of an Internet-delivered lifestyle physical activity intervention for improving sexual dysfunction in women with MS. The research proposed, if successful, will provide evidence for the efficacy of physical activity as a translatable approach for managing sexual dysfunction among women with MS.

NCT ID: NCT04768088 Not yet recruiting - Knee Injuries Clinical Trials

Training of Falling Techniques on Landing Mechanics

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

The overall purpose of this study is to quantify the effect and retention of one-week training of falling techniques on landing biomechanics associated with anterior cruciate ligament (ACL) loading compared to soft-landing techniques in young recreational athletes. The secondary purpose is to assess the safety of the training program. Aim 1: To quantify the effect of one-week training of falling techniques on landing biomechanics during forward, lateral, vertical, and diagonal landings compared to soft-landing techniques. We hypothesize that falling techniques will result in increased knee flexion angles and decreased landing forces, knee abduction and internal rotation angles, and knee moments for all landing directions compared to soft-landing techniques immediately after the training. Aim 2: To assess the retention effects of the falling techniques on landing biomechanics compared to soft landings. We hypothesize that the effects of falling techniques on ACL loading variables will be more highly retained compared to soft-landing techniques two weeks after the training. Aim 3: To identify the safety of the training program. We hypothesize that participants can complete the training without suffering minor, moderate, or major injuries, while occasional minor bruises might be observed.

NCT ID: NCT04760860 Not yet recruiting - Clinical trials for Dementia With Lewy Bodies

Terazosin for Dementia With Lewy Bodies

TZ-DLB
Start date: October 2024
Phase: Phase 1/Phase 2
Study type: Interventional

The TZ-DLB trial will be a 3:2 (active:placebo) randomized, double-blind, placebo-controlled Pilot trial to evaluate the tolerability of terazosin for the treatment of dementia with Lewy bodies.

NCT ID: NCT04760847 Not yet recruiting - Pancreatitis Clinical Trials

Intermittent Fasting for Pancreatitis

IFPanc
Start date: July 7, 2024
Phase: N/A
Study type: Interventional

The purpose of this research is to compare intermittent fasting with a standard diet approach for improving the quality of life related to your pancreas disease. Our hope is to improve your symptoms and prevent you from needing to go into the hospital for pancreas-related issues.