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Clavicle Fracture clinical trials

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NCT ID: NCT06276218 Recruiting - Clavicle Fracture Clinical Trials

Efficacy of Self - Adjustable Clavicular Brace Versus Standard Clavicular Brace for Treatment of Mid Shaft Clavicle Fracture: A Randomized Controlled Study

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

A randomized control trial was conducted to compare the outcomes of conservative management for closed midshaft clavicular fractures using self-adjustable clavicular brace and standard clavicular brace.

NCT ID: NCT06106399 Recruiting - Clavicle Fracture Clinical Trials

US Guided WALLANT vs CPB Block for Clavicle Surgery

WALANT-CPB
Start date: August 1, 2023
Phase: N/A
Study type: Interventional

The clavicle is frequently fractured bone. regional anesthesia (RA) for clavicle surgery is always challenging due t complex innervation from the two plexuses (cervical and brachial). various RA techniques described for clavicle surgery include plexus blocks, fascial plane blocks,and truncal blocks.

NCT ID: NCT05867355 Recruiting - Clavicle Fracture Clinical Trials

Surgically Treated Displaced Mid-diaphyseal Clavicle Fractures

Start date: March 22, 2021
Phase:
Study type: Observational

This prospective, multi-centre study aims to determine clinical, radiographic, and patient-reported outcomes (PROMs) following surgical fixation of displaced mid-diaphyseal clavicle fractures and to compare implant removal rates between techniques within 2-years of the procedure.

NCT ID: NCT05810129 Recruiting - Clavicle Fracture Clinical Trials

Crossed Education in Relation to Muscle Mass in Patients Operated of Clavicular Fracture

crossed1
Start date: May 2, 2023
Phase: N/A
Study type: Interventional

The immobilization process after an operation or injury in the upper extremity causes a loss of muscle mass and strength of 0.2% and 1.3% per day, respectively. Currently, the use of cross-education, which is unilateral training in the uninjured limb, during the immobilization period, is expanding, demonstrating a magnitude of strength gain in the immobilized limb from 8% to 77% of the mean of strength of the trained limb. Despite the evidenced benefits of cross-education in unilateral injuries such as distal radius fracture, anterior cruciate ligament injury, and knee replacement, very little is known about this effect in shoulder immobilization after clavicle fracture.

NCT ID: NCT05231343 Recruiting - Clavicle Fracture Clinical Trials

Comparing Dual Mini-fragment Plating to Single Precontoured Plating of Acute Midshaft Clavicle Fractures Trial

COMPACT
Start date: April 4, 2022
Phase: N/A
Study type: Interventional

The rate of surgical fixation of fractures of the collarbone (i.e., midshaft clavicle) has exponentially increased in recent years; however, the rate of repeat procedures for removal of these implants (i.e., plates) due to irritation remains high. Despite technological advances in implant design, nearly one in four patients with a surgically fixed collarbone ultimately undergoes removal of their implant. More recently, there has been a growing body of literature demonstrating the effectiveness of using two smaller caliber plates, which have been found to have similar rates of implant removal. As such, the proposed randomized clinical trial seeks to be the first level I study to directly compare dual mini-fragment plating of acute displaced midshaft clavicle fractures to single precontoured plating. The investigators hypothesize that dual mini-fragment plating will result in lower rates of reoperation with similar rates of union and complication.

NCT ID: NCT04250415 Recruiting - Clavicle Fracture Clinical Trials

Multi-Center Adolescent Clavicle Fracture Trial: Operative vs. Non-Operative Treatment

FACTS
Start date: March 11, 2013
Phase:
Study type: Observational [Patient Registry]

Investigators from eight tertiary care, level 1 pediatric trauma centers have developed a protocol for the establishment of a formal, prospective multi-center adolescent clavicle registry, with designs for standardized radiographic assessment and the prospective collection of validated outcome measures and complications data, for all patients, ages 10-18, treated for clavicle shaft fractures, operatively and non-operatively. Eventually, the investigators would like to do comparative analysis for the operative and non-operative treatment arms, with additional sub-stratified analyses performed within these treatment arms by age and activity level. Among the primary goals of research projects stemming from the first arm of this registry, FACTS A, is to explore the hypothesis that non-operative treatment is associated with lower costs, greater safety, and equivalent or superior outcomes, compared with operative treatment, despite a national trend towards increasing surgical treatment. The second arm of the registry, FACTS B, will continue to investigate the same hypotheses, excluding cost outcomes, in patients only with completely displaced midshaft clavicle fractures.

NCT ID: NCT04161534 Recruiting - Clavicle Fracture Clinical Trials

KT Tape for Pediatric Clavicle Fractures

Start date: October 1, 2020
Phase: N/A
Study type: Interventional

Clavicle fractures in children are mostly managed non-operatively since they have an overall high union rate (95%) and a "good" functional outcome following nonoperative treatment. However, the downside of such a conservative approach is that patients have to live with pain and disability until the fracture heals. To minimize this, fractures are usually immobilized with a sling. There have been no studies looking at clavicle fractures treated with kinesiology (elastic) tape. No adverse effects (skin irritation, redness, etc.) are observed with the application of this tape. Elastic tape has previously been examined regarding muscular advantages rather than for healing fractures. Since this tape should immobilize fractures better than a sling, patients should experience less pain and disability associated with their fracture.

NCT ID: NCT03094481 Recruiting - Clavicle Fracture Clinical Trials

Interscalene vs. Superficial Cervical Block vs. Combination for Analgesia After Clavicle Fracture

Start date: October 21, 2016
Phase: N/A
Study type: Interventional

The optimal analgesic peripheral nerve block (or combinations thereof) are undefined for clavicle fractures, the most frequent fracture in the human population. This goal of this study is to determine whether interscalene block (ISB), superficial cervical plexus block (SCPB), or both provide the best analgesia for lateral and midshaft clavicular fractures, respectively.