Efficacy of Ultrasound-Guided Needle Knife Release for Trigger Finger
Recruiting now · Not applicable
Conditions studied: Trigger Finger
In brief
Efficacy of ultrasound-guided tri-directional needle knife release in treating patients with trigger finger. The study evaluates safety, effectiveness, and recovery outcomes of a minimally invasive procedure compared to conventional approaches.
Key facts
- Study ID
- NCT06788860
- Run by
- Mohamed Maher Ismail Ahmed Elashmawy
- People needed
- 46
- Starts
- 2025-01-20
- Expected to finish
- 2025-10-29
- Last updated by the study team
- 2025-01-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Idiopathic TF at the level of A1 pulley
- Trigger finger of Green's grades II or III or IV (moderate to severe)
- Symptoms persist for at least three months despite conservative treatments.
- Ability to provide informed consent and comply with follow-up requirements.
You may not qualify if…
- Patients with secondary causes of TF like diabetes mellitus, rheumatoid arthritis, gout, hypothyroidism, amyloidosis, and sarcoidosis.
- Patients with TF of Green's grade I.
- Previous surgical intervention on the affected digit.
- Allergy or contraindication to local anesthetics.
- Pregnancy or lactation.
- Inability to comply with follow-up assessments.
Where it is running
- Mansoura University Hospital — Al Mansurah, Dakahlia Governorate, Egypt (enrolling)
Full record on ClinicalTrials.gov
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