Using mechanical devices to manage pain and swelling after wrist surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized controlled trial evaluates the effectiveness of mechanical modalities, specifically continuous passive motion (CPM) and intermittent pneumatic compression (IPC), in addition to standard care for patients recovering from distal radius fracture (DRF) fixation. The study aims to measure outcomes such as edema volume and pain intensity at six weeks post-operation, along with secondary outcomes like range of motion and grip strength. Participants will be monitored for adverse events throughout the study period.

Why it matters

Who can join: the full rules

Inclusion Criteria:

Adults aged 18 years or older. Undergoing surgical treatment for distal radius fracture with stable internal fixation.

Able to initiate formal rehabilitation approximately 2 weeks postoperatively. Willing and able to attend in-clinic therapy sessions at the outpatient hand therapy center.

Exclusion Criteria:

Unstable fixation or need for further surgical intervention. Pre-existing conditions that would significantly affect upper limb function (e.g., severe arthritis, neurological disorders).

History of skin conditions or allergies that contraindicate the use of mechanical devices.

Any contraindication to mechanical modalities (for example, severe peripheral vascular disease).

Inability to comply with study procedures or follow-up visits. Pregnant or breastfeeding individuals.

Where it's running

• Faculty of Physical Therapy, Al Hayah University
  Cairo, Egypt Recruiting

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Cannulated screws versus K-wires for fixing distal radius (wrist) fractures

  This study will test whether cannulated screws or K-wires lead to better arm function and fewer complications in adults (18–60) with displaced extra-articular distal radius fractures.

  Recruiting Sohag University · Sohag, Naser City · NCT07523386

• Fu's subcutaneous needling with rehabilitation to help heal distal radius fractures after closed reduction

  This trial will test whether adding Fu's subcutaneous needling to standard rehabilitation helps adults (18–85) heal distal radius fractures after closed reduction and splinting.

  Recruiting Guangzhou University of Chinese Medicine · Guangzhou, Guangdong · NCT07054463

• Comparing two types of splints for wrist stiffness after a fracture

  This study is testing which type of splint, static progressive or dynamic, helps adults with wrist stiffness after a fracture feel better and move their wrist more easily.

  Recruiting Al Hayah University In Cairo · Cairo · NCT06913933

• Comparing rehabilitation methods for wrist fractures in younger adults

  This study is testing three different rehab methods for wrist fractures in younger adults to see which one helps them recover better.

  Recruiting Al Hayah University In Cairo · Cairo · NCT06913894

• Evaluating radiological criteria for stability in wrist fractures

  This study tests if certain X-ray and CT scan results can help doctors decide if adults with wrist fractures need surgery after a closed reduction.

  Recruiting Oslo University Hospital · Oslo, Oslo · NCT06617780

• Long-term safety evaluation of NVDX3 treatment

  This study is testing the long-term safety of the NVDX3 treatment in patients who have already received it, by checking in with them every year for 10 years to see if they experience any problems.

  Recruiting Phase 1/2 Novadip Biosciences · Luxembourg · NCT06532253

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.