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Fractures, Stress clinical trials

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NCT ID: NCT05792202 Recruiting - Clinical trials for Full Rotator Cuff Tear

Combined Microfracture Procedure Promotes Tendon Healing

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

This study is a prospective randomized controlled study of Combined microfracture procedure promotes tendon healing during double raw repair for full tear rotator cuff. The patients with rotator cuff tear were randomly divided into groups before the operation. The patients were followed up before and 6 weeks, 3 months, 6 months, 12 months after surgery. In different time periods, the quantitative and qualitative indicators including pain, functional score, muscle strength, MRI performance, etc. were compared between groups at the same time period to evaluate the difference in the effect of Crimson duvet procedure with Greenhouse procedure on the treatment of rotator cuff.

NCT ID: NCT05786079 Completed - Clinical trials for Tibial Stress Fracture

Effects of Footstrike Transition on Tibial Stress Fracture Risk

Start date: June 1, 2016
Phase: N/A
Study type: Interventional

Biomechanical literature suggests that runners who utilize a mid or forefoot strike pattern may suffer from a reduced incidence of chronic injuries compared to a rearfoot strike. This investigation examined the effects of a 10-week footstrike transition intervention on tibial stress fracture risk in runners.

NCT ID: NCT05741983 Withdrawn - Clinical trials for Osteochondral Lesion of Talus

AMIC vs. MFx in the Ankle

AMARTA
Start date: April 28, 2023
Phase: N/A
Study type: Interventional

This clinical investigation is a prospective, double blind, single-centre, randomised controlled trial comparing arthroscopic autologous matrix induced chondrogenesis (AMIC®) to microfracture alone in the treatment of osteochondral and chondral lesion in the ankle to evaluate effectiveness, performance and safety of AMIC® procedure versus microfracture (MFx).

NCT ID: NCT05694585 Not yet recruiting - Airway Obstruction Clinical Trials

Effect of Esmolol on Perioperative Stress Reaction

Start date: February 1, 2023
Phase: Phase 4
Study type: Interventional

The goal of this clinical trial is to observe the effect of low dose continuous infusion of esmolol on perioperative stress response in patients undergoing airway intervention .

NCT ID: NCT05685368 Recruiting - Quality of Life Clinical Trials

Acceptance and Commitment Therapy (ACT) for Combating the Effects of Race-Related Stress Among Black Adolescents

Start date: August 28, 2023
Phase: N/A
Study type: Interventional

The current study seeks to build on previous research that demonstrates the efficacy of Acceptance and Commitment Therapy in combating stigma by investigating the feasibility and acceptability of a protocol to support Black adolescents and young adults in coping with race related stress. The study will consist of a small, purposeful, non-randomized sample (N = 30) of clients enrolled into a 10-session Acceptance and Commitment Therapy group. The group will be offered as part of regular clinical care at the Division of Adolescent and Young Adult Medicine. Three consecutive groups will be run with approximately 8-10 participants in each group over the next year.

NCT ID: NCT05624164 Recruiting - Rotator Cuff Tears Clinical Trials

Microfracture at Proximal Humerus Lateral to Footprint Could Enhance the Rotator Cuff Healing

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

The goal of this clinical trial is to test whether there is any effect on rotator cuff healing by making microfracture at the lateral side of the footprint. The main question it aims to answer are: - [whether the lateralized microfracture could decrease the retear rate after arthroscopy rotator cuff repair.] - [whether the lateralized microfracture could improve the functional recovery after arthroscopy rotator cuff repair.] Participants with medium to larger size rotator cuff tears will be randomly assigned to the study group treated with lateralized microfracture immediately after arthroscopy rotator cuff repair or the control group treated with conventional arthroscopy rotator cuff repair without microfracture.

NCT ID: NCT05521919 Recruiting - Stress Reaction Clinical Trials

Acute Plasma Abeta Responses to Stress

Start date: February 14, 2024
Phase: N/A
Study type: Interventional

Research has shown that activation of the sympathetic nervous system for extended periods or during certain times in life can increase the risk for Alzheimer's disease. Some research in animal models show that acute activation of the sympathetic nervous system through stress exposure can increase certain Alzheimer's disease-related biomarkers, such as amyloid-beta, within hours of exposure. However, how acute sympathetic nervous system activation via stress exposure affects amyloid-beta levels in humans has yet to be examined. In this study, the investigators will examine whether brief increases in sympathetic activation result in immediate changes in plasma amyloid-beta levels in the five hours after exposure.

NCT ID: NCT05512013 Completed - Bone Resorption Clinical Trials

The Effects of NSAIDs on Bone Metabolism Following Exercise

Start date: February 15, 2022
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the effects of a single dose of non-steroidal anti-inflammatory drugs on post-exercise markers of bone and muscle metabolism.

NCT ID: NCT05490251 Recruiting - Smoking Cessation Clinical Trials

Translational Research Center in Lung Cancer Disparities (TRACER) Project 2

TRACER
Start date: June 1, 2024
Phase:
Study type: Observational

The purpose of this study is to examine racial differences in smoking behaviors and stress responses between African American and white male smokers.

NCT ID: NCT05426356 Active, not recruiting - Osteoporosis Clinical Trials

Sacral Fracture Fusion/Fixation for Rapid Rehabilitation

SAFFRON
Start date: September 18, 2022
Phase: N/A
Study type: Interventional

To determine the safety and efficacy of concomitant sacral fracture fixation and sacroiliac (SI) joint fusion vs. non-surgical management for patients with debilitating sacral fragility or insufficiency fractures