Mechanical Modalities vs. Standard Care for Edema and Pain Management After DRF Fixation
Recruiting now · Not applicable
Conditions studied: Distal Radius Fractures
In brief
This single-blinded, randomized controlled trial (RCT) will evaluate the added benefit of mechanical modalities (continuous passive motion (CPM) and intermittent pneumatic compression (IPC)) when integrated into standard therapy for managing postoperative edema and pain in patients undergoing distal radius fracture (DRF) fixation. The primary outcomes are edema volume (measured via volumeter) and pain intensity (Numeric Pain Rating Scale, NPRS) at 6 weeks post-operation. Secondary outcomes include wrist/forearm range of motion (ROM), grip strength, Patient-Rated Wrist Evaluation (PRWE), and adverse events.
Key facts
- Study ID
- NCT06913920
- Run by
- Al Hayah University In Cairo
- People needed
- 50
- Starts
- 2025-04-15
- Expected to finish
- 2026-01-15
- Last updated by the study team
- 2025-04-06
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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.
You may not qualify if…
- 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 is running
- Faculty of Physical Therapy, Al Hayah University — Cairo, Egypt (enrolling)
Full record on ClinicalTrials.gov
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