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Elbow Fracture clinical trials

View clinical trials related to Elbow Fracture.

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NCT ID: NCT04738318 Terminated - Elbow Fracture Clinical Trials

Steroid Administration for Articular Fractures of the Elbow (SAFE Trial)

SAFE
Start date: June 16, 2022
Phase: Phase 4
Study type: Interventional

The primary purpose of this study is to determine if perioperative glucocorticoid administration (IV intra-operative followed by a post-operative oral taper course) improves post-operative range of motion in a patient population that has sustained an intra-articular elbow fracture(s) (radial head, proximal ulna, distal humerus, or combined) that required operative fixation.

NCT ID: NCT04648488 Not yet recruiting - Elbow Fracture Clinical Trials

Early Mobilisation After Surgery in Patients With Elbow Fracture-dislocation

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

The purpose with the study is to evalute if early mobilsation after surgery in patients vid elbow frakture-dislocation may lead to better armfunction and reduce common complications as stiffnes in the elbow. After surgery patients will be randomised to either early mobilisation (exercise treatment 3 Days after surgery) or ordinary treatment (plaster and exercise treatment 3 weeks after surgery).

NCT ID: NCT04642807 Recruiting - Trauma Clinical Trials

Management of Type 1 Supracondylar Humeral Fractures

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

This study compares the clinical outcomes of treating pediatric Type 1 supracondylar fracture with a long arm soft cast and no clinical or radiographic follow-up versus the standard treatment in a long arm cast with clinical follow-up. This is the first multicenter randomized control trial looking at the clinical effectiveness, safety and parental satisfaction of managing inherently stable Type I supracondylar fractures without clinical or radiological follow-up. If found to be safe; children can be managed effectively without in-person follow-up, freeing clinic appointments to children on the waiting list and in these COVID times avoiding unnecessary contacts.

NCT ID: NCT04634305 Active, not recruiting - Elbow Fracture Clinical Trials

Clinical and Functional Results After Total Elbow Arthroplasty

Start date: January 1, 2004
Phase:
Study type: Observational [Patient Registry]

Analysis of clinical and functional outcomes after a total elbow arthrosplasty, all indications combined, with a minimum follow up of 24 months The hypothesis is that there a significant improvement after an elbow replacement, no matter what the surgery indication is

NCT ID: NCT04571905 Completed - Elbow Fracture Clinical Trials

MagnezixKids Study

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

The overall objective of the study is to describe the outcomes of osteosyn-thesis with magnesium based screws in children with a primary or second-ary (within 7 days from trauma) dislocated fracture of the Epicondyles ul-naris or Condylus radialis, and to compare them with outcomes of conven-tional osteosynthesis using steel screws. If our results suggest non-inferiority of osteosynthesis with magnesium-based screws, the procedure could be tested formally in a subsequent full-size study.

NCT ID: NCT03969277 Completed - Pain, Postoperative Clinical Trials

Graded Motor Imagery in Elbow Limitation

Start date: October 15, 2019
Phase: N/A
Study type: Interventional

This randomized-controlled trial aims to investigate the efficacy of Graded Motor Imagery (GMI) on function, pain, and range of motion (ROM) in patients with a posttraumatic stiff elbow.

NCT ID: NCT03582176 Active, not recruiting - Elbow Fracture Clinical Trials

PrEvention of Posttraumatic Joint contractuRes With Ketotifen 2

PERK2
Start date: April 26, 2019
Phase: Phase 3
Study type: Interventional

PrEvention of posttraumatic contractuRes with Ketotifen 2 (PERK 2) is a Phase III randomized, controlled, double blinded multicenter trial with 3 parallel groups (Ketotifen 2 mg or 5 mg or lactose placebo twice daily orally for 6 weeks) and a primary endpoint of elbow extension-flexion range of motion (ROM) arc at 12 weeks post-randomization.

NCT ID: NCT03379935 Completed - Clinical trials for Arthroplasty Complications

Radial Head Arthroplasty A Clinical and Radiological Comparison of Monopolar and Bipolar Radial Head Arthroplasty

RHA
Start date: January 1, 2017
Phase: N/A
Study type: Observational

Fractures of the radial head are among the most common fractures in the elbow and represent one-third of all elbow fractures.This retrospective cohort study was performed between 2004 and 2014 at Sundsvall and Umeå University hospital, Sweden. All patients who were operated on between 2004 and 2014 with a radial head arthroplasty for an acute or sequelae due to a caput radii fracture.The aim of this study is to evaluate clinical or radiological differences between patients treated with a unipolar or bipolar radial head arthroplasty.

NCT ID: NCT03302533 Completed - Elbow Fracture Clinical Trials

Can Secondary Total Elbow Arthroplasty After Failed Internal Fixation or Non-operative Treatment of Distal Humeral Fractures Achieve Equal Results as Primary Arthroplasty?

Start date: January 21, 2013
Phase: N/A
Study type: Observational

Total elbow arthroplasty (TEA) results in immediate pain release with good functional results after distal humerus fractures. But still open reduction and internal fixation is recommended as treatment of choise due to a lifelong loading limitiation, unknown implant survival and problematic revision surgery after TEA. The purpose of this study was to compare functional results and complication rates after primary total elbow arthroplasty (TEA) and TEA after failed reconstruction or non-operative treatment (secondary TEA) in the treatment of distal humerus fractures. We hypothesised that clinical and functional results are better for primary TEA with less complications.

NCT ID: NCT03161782 Completed - Postoperative Pain Clinical Trials

The Efficacy of Different Types of Stretching on Range of Motion, Pain and Function in Elbow Limitation

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

The aim of the study is to compare the efficacy of Proprioceptive Neuromuscular Facilitation (PNF) stretching and static stretching on range of motion (ROM), pain and function in elbow limitation.