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Extremity Injury clinical trials

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NCT ID: NCT06326827 Not yet recruiting - Orthopedic Disorder Clinical Trials

In'Oss™ (MBCP® Putty) Ortho

Start date: September 2024
Phase:
Study type: Observational

Study of the osteoconductive potential of the injectable bone substitute In'Oss™ (MBCP® Putty) in the filling of orthopaedic bone defects to collect Post-Market Clinical Follow-up (PMCF) data for the CE-marked In'Oss™ (MBCP® Putty) device in the orthopaedic trauma surgery

NCT ID: NCT04216225 Enrolling by invitation - Extremity Injury Clinical Trials

Pre-hospital Tourniquet in Extremity Injury

Start date: November 1, 2018
Phase:
Study type: Observational

2.1. Objective: • Primary Objective: To compare outcomes of patients with extremity injuries presenting with or without pre-hospital tourniquet placement. 2.2. Study Outcome Measures - Primary Outcome: Incidence of arrival in shock (SBP <90) - Secondary Outcomes: Demographics, comorbidities, mechanism of injury, cause of injury, diagnosis codes, procedure codes, Injury Severity Scale, Abbreviated Injury Scale, operative management vs. non-operative management, radiologic findings, pathologic findings, tourniquet effectiveness (as determined both subjectively by trauma surgeon and objectively by presence vs. absence of pulse below level of tourniquet application), total number of units of blood products transfused within first 24 hrs, total number of units of blood products for index admission, type of blood products or other fluid given, hospital length of stay, ICU length of stay, ventilator days, infectious complications, other complications, discharge disposition, 24 hr mortality, overall mortality.

NCT ID: NCT03891966 Completed - Extremity Injury Clinical Trials

Upper Extremity Post-op Splints: Do They Improve Post-operative Pain?

Start date: November 8, 2018
Phase: N/A
Study type: Interventional

The goal of this study is to determine if applying a rigid splint helps to reduce pain following operative fixation of upper extremity fractures. Orthopedic trauma surgeons currently vary in their application of rigid post-operative splints versus soft dressings after certain surgical procedures based on personal preference. In this study, 100 patients undergoing operative fixation of isolated both bone forearm, radial head, olecranon, distal humerus, or humeral shaft fractures will either receive a splint or soft dressing post-operatively. Their pain, medication usage and function will be tracked over the 2- week postoperative period to see if splinting has any impact on outcomes.

NCT ID: NCT01616342 Recruiting - Extremity Injury Clinical Trials

Management of Chronic Pain in Military Patients With Injuries Sustained During Active Duty

War Wounded
Start date: December 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the degree to which spinal cord stimulation added to comprehensive medical management can provide increased relief of chronic pain in patients with injuries sustained while on active military duty, measured by patient assessments of pain.

NCT ID: NCT01497678 Withdrawn - Muscle Injury Clinical Trials

Musculotendinous Tissue Unit Repair and Reinforcement (MTURR) Coordinating Center

MTURR
Start date: March 2013
Phase: N/A
Study type: Interventional

The objective of the study is to assess mechanical strength and function in subjects undergoing Musculotendinous Tissue Unit Repair and Reinforcement (MTURR) with the use of biologic scaffolds for the restoration of both mechanical strength and function in these subjects. This study will formally evaluate healing and return of function after an extracellular matrix device implantation in 40 male and female subjects participating at 4-5 military sites who suffer from injury with loss of skeletal muscle tissue. The University of Pittsburgh under the Department of Plastic and Reconstructive Surgery is the Coordinating Center for this multi-site study.

NCT ID: NCT01292876 Completed - Muscle Injury Clinical Trials

Musculotendinous Tissue Repair Unit and Reinforcement (MTURR)

MTURR
Start date: December 2010
Phase: N/A
Study type: Interventional

The objective of the study is to assess mechanical strength and function in subjects undergoing Musculotendinous Tissue Unit Repair and Reinforcement (MTURR) with the use of biologic scaffolds for the restoration of both mechanical strength and function in these subjects. This study formally evaluated healing and return of function after an extracellular matrix device implantation in 17 male and female subjects participating at the University of Pittsburgh under the Department of Plastic and Reconstructive Surgery who suffer from injury with loss of skeletal muscle tissue.