Early Postoperative Function After Open Versus Ultrasound-Guided Trigger Finger Release (NCT07364695) | Clinical Trial Compass
CompletedNot Applicable
Early Postoperative Function After Open Versus Ultrasound-Guided Trigger Finger Release
United States60 participantsStarted 2023-06-20
Plain-language summary
Clinical outcomes after open trigger finger release are excellent. Minimally invasive techiques with ultrasound guidance theoretically offer advantages for faster recovery but this technique has not been compared prospectively with the standard of care (open trigger release). This study aims to prospectively analyze patient-reported outcomes in patients undergoing open vs. ultrasound-guided trigger finger release.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* undergoing trigger finger release for the index through small fingers due to symptoms refractory to conservative treatment and elected for surgical intervention through shared decision-making
* English-speaking adults (≥18 years of age)
* Patients with inflammatory arthritis were included if their diagnosis had been established ≥5 years prior without exacerbations in the past 5 years. Those on immunomodulatory therapy were required to have been on a stable regimen for ≥5 years without flare-ups.
Exclusion Criteria:
* prior surgery on the affected finger
* corticosteroid injection in the affected hand within 6 weeks
* additional hand or wrist pathology requiring concurrent surgery
* symptomatic trigger finger in the contralateral extremity
* prior surgical pulley release in either hand within 6 months of enrollment
* Systemic inflammatory disease (e.g., rheumatoid arthritis, lupus) not controlled
* inflammatory arthritis if diagnosis established \<5 years, exacerbation within the past 5 years, or modifications to immunomodulatory therapy within 5 years of enrollment
* Amyloidosis
* Diabetes not controlled by a stable dose of medication over the past three months
* Pregnant or planning pregnancy in the next 6 months
* Workers' compensation subjects
* Inability to provide a legally acceptable Informed Consent Form and/or comply with all follow-up requirements, including patients who do not speak English
* other medical, social, or psychological condition…
What they're measuring
1
Activities of Daily Living (Study-specific questionnaire)
Timeframe: From enrollment to final follow-up at 6 months
2
Pain on the Visual Analogue Scale
Timeframe: From enrollment to final follow-up at 6 months