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Distal Radius Fracture clinical trials

View clinical trials related to Distal Radius Fracture.

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NCT ID: NCT05332080 Completed - Clinical trials for Distal Radius Fracture

Telerehabilitation in Distal Radius Fracture

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

Objective: To determine the effectiveness of telerehabilitation versus supervised therapy in the functional recovery of patients with distal radius fracture. Design: A randomized, controlled, parallel-treatment trial protocol was performed to compare functional recovery after a telerehabilitation program vs supervised rehabilitation in patients with distal radius fracture. Setting: Participants: A total of 91 patients with distal radius fractures grades AO23 A and B. Interventions: the supervised rehabilitation group received for two weeks a 10-session program that included external heat application, stretching, mobilization, strengthening, and occupational therapy. The telerehabilitation group was given instructions to apply hydrotherapy, perform mobility and wrist and hand strengthening exercises for four weeks, using the Moodle application on their cell phone. Main outcomes measures: Outcome measures were measured at the time of admission to rehabilitation and 1, 3, and 6 months; at each follow-up visit, functionality, active range of motion, fist grip strength, quality of life and pain were measured. Results: When the results obtained at the beginning and at six months were compared, both groups presented statistically significant changes in the clinical variables analyzed but with greater functionality in the telerehabilitation group.

NCT ID: NCT05318729 Not yet recruiting - Postoperative Pain Clinical Trials

Use of a Vibration Tool for Postoperative Pain Control in Distal Radius Fractures

Start date: March 2025
Phase: N/A
Study type: Interventional

The purpose of this research study is to determine if using a vibration tool improves pain control after surgical treatment of distal radius fracture. Additionally, the investigators would like to determine if this tool has any impact on consumption of pain medications postoperatively.

NCT ID: NCT05274113 Enrolling by invitation - Post Operative Pain Clinical Trials

Low Dose Dexamethasone for Distal Radius Fractures

Start date: March 10, 2022
Phase: Phase 3
Study type: Interventional

The addition of the steroid dexamethasone to a single injection of local anesthetic has been shown to significantly prolong the duration of peripheral nerve blockade compared to local anesthetic alone. This allows for improved post-operative pain scores and reduces opioid use in the early post-operative period. However, the use of a steroid adjuvant in regional nerve blocks is generally not considered standard of care, and there is considerable variation among anesthesiologists regarding preferred formulations and the role of adjuvants in regional anesthesia. A recent study from our institution demonstrated the effectiveness of dexamethasone directly mixed with local anesthetic at multiple doses compared to placebo for upper extremity surgery. With this prospective randomized controlled blinded trial, we hope to definitively establish which method of adjuvant dexamethasone administration is superior in extending the effects of a brachial plexus nerve block.

NCT ID: NCT05264675 Recruiting - Clinical trials for Distal Radius Fracture

Functional Outcome After EPL-rupture After Distal Radius Fracture

Start date: January 1, 2022
Phase:
Study type: Observational

Rupture of the extensor pollicis longus, (EPL) is a common complication after distal radius fractures. A rupture prevents the thumb extension, which in turn has a negative impact on hand function. An EPL-rupture can either be surgically treated by primary suture, which means that the ends of the tendon are sutured. This is however not recommended if the tendon is weakened. In such cases the rupture can be treated by a transfer of, most often, extensor indicis proprius (EIP) to the thumb. Distal radius fractures are common and a rupture of the EPL-tendon is a known complication thar interferes with hand function and therefore more studies on this patient group are warranted. The aim of this prospective study is to compare regaining of thumb function after surgery, with the non-injured side, after primary suture and EIP-transfer after EPL-rupture as a complication following distal radius fracture.

NCT ID: NCT05237531 Terminated - Clinical trials for Distal Radius Fracture

Preoperative Education in Hand and Wrist Surgery

Start date: March 15, 2022
Phase: N/A
Study type: Interventional

This study will compare opioid consumption in patients undergoing outpatient surgical fixation of distal radius fractures with and without standardized preoperative education at Grady Memorial Hospital.

NCT ID: NCT05215236 Enrolling by invitation - Clinical trials for Distal Radius Fracture

Opiate Sparing Protocol Randomized Controlled Trial in Open Distal Radius Fracture Repair

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

A comparison of oral morphine equivalents between an opiate sparing cohort and an opiate based cohort following open reduction internal fixation of a distal radius fracture.

NCT ID: NCT05188040 Completed - Clinical trials for Distal Radius Fracture

Effectiveness of Virtual Reality in Hand Therapy

Start date: May 16, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the use of Virtual Reality as an intervention for patients following specific hand injuries will positively affect patients with decreased hand function and reduce pain and improve outcomes. Participants will be recruited from 3 different clinics in central Kentucky.

NCT ID: NCT05175118 Not yet recruiting - Clinical trials for Distal Radius Fracture

Minimally Invasive Fixation for Distal Radius Fractures

DRF
Start date: December 20, 2024
Phase: N/A
Study type: Interventional

Minimally invasive surgery avoids the tissue damage and impairment of physiological function caused by open surgery because of its precise location techniques and can effectively promote the early recovery of wrist function. Under conditions of no cutting of fracture fragments, no blood supply compromise in the fracture fragments

NCT ID: NCT05159310 Recruiting - Clinical trials for Distal Radius Fracture

Cast Vs Splint in Distal Radius Fractures

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

This study will evaluate and compare the efficacy of 2 commonly-used methods of fracture immobilisation: (1) Fiberglass cast, and (2) Thermoplastic splint. Both these devices are externally applied and provide pain relief while immobilising the fracture in an acceptable position. Casts and splints are both established devices in routine clinical use.

NCT ID: NCT05150925 Recruiting - Clinical trials for Distal Radius Fracture

Immediate Mobilization Versus 2 Weeks Cast Immobilization After Distal Radius Fracture Treated With Volar Locking Plate

LIMPER-DRF
Start date: December 1, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to analyze total lenght of the sick leace and functional outcome (PRWE) at 2 months between 2 weeks casting and immediate mobilization following volar plating for a DRF.