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 range
18 Years
Sex
ALL
See this in plain English?
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…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
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