Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to compare the effectiveness of resection of one or both slips of the flexor digitorum superficialis tendon versus the A1 pulley division.


Clinical Trial Description

The preoperative visit occurred a number of weeks or months prior to surgery. Surgeons from the Centre de la main at the CHUV in Lausanne recruited the subjects during their consultations. During this initial visit, the patient was asked about his problem, his general health and a clinical examination (including range of motion of finger joints, pulp-to-palm distance, pain evaluated with a VAS) was performed. Once the diagnosis of trigger finger was established, the inclusion and exclusion criteria were evaluated. If the eligibility criteria were fulfilled, the patients were offered to be part of the study. They received oral and written information about the study and the surgeons gave further explanation if needed. On the surgery day, the signed consent form was recovered. Participants were randomized in two groups according to a computer-generated list ranging from 01 to 60 (www.randomization.com). Surgery was then performed according to the method chosen by randomization. The possible occurrence of adverse effects during surgery was monitored. All information was recorded on the case report forms. The first postoperative visit occurred 1 week ± 3 days after surgery. The surgeons evaluated the wound to exclude the presence of postoperative complication (infection, hematoma, nerve or tendon injury) and answer any question the patient could have. Range of motion and pain were recorded. All information was recorded on the case report forms. The second postoperative visit occurred 4 weeks ± 5 days after surgery. The appointment was conducted in the same way as the previous one. Patients could choose to be withdrawn from the study at any point. The follow-up was similar to that of patients included in the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04675892
Study type Interventional
Source Centre Hospitalier Universitaire Vaudois
Contact Thierry Christen, MD
Phone +41(0)795561287
Email thierry.christen@chuv.ch
Status Recruiting
Phase N/A
Start date November 1, 2018
Completion date December 1, 2024

See also
  Status Clinical Trial Phase
Completed NCT04094389 - Comparison of Trigger Finger Orthotic Wearing Schedules N/A
Completed NCT05435950 - Clinical Investigation on Safety, Performance and Effectiveness of Sono-instruments N/A
Completed NCT04900220 - Differences in Flare Reaction Incidence and Intensity Following Trigger Finger Injections Phase 4
Completed NCT06401473 - Using the Gate Control Theory of Pain to Decrease Pain During Trigger Finger Corticosteroid Injections N/A
Completed NCT04354415 - Tourniquet vs. No Tourniquet for Carpal Tunnel and Trigger Finger Release N/A
Recruiting NCT06296017 - Effectiveness of Conservative Interventions in the Treatment of Trigger Finger N/A
Completed NCT06288685 - Percutaneous Trigger Finger Release Concomitant Steroid Injection Versus Percutaneous Trigger Finger Release Alone Phase 3
Completed NCT06382623 - Efficacies of Different Managements in Patients With Trigger Finger
Active, not recruiting NCT04568993 - The TriggerHappy Trial N/A
Completed NCT04023695 - Trigger Finger Corticosteroid Injection With and Without Local Anesthetic Phase 4
Recruiting NCT04645303 - Injection of Hyaluronic Acid Versus Corticosteroid for Treatment of Trigger Finger Early Phase 1
Recruiting NCT03156829 - Effectiveness of Cortisone Injection and Splinting for Trigger Finger Phase 4
Completed NCT01987115 - Comparison of Fascial Manipulation With Traditional Physiotherapy for the Treatment of Trigger Fingers N/A
Completed NCT01950793 - A Comparison Between Sonoguided Injection Corticosteroid and Hyaluronic Acid Injection in Treatment of Trigger Finger N/A
Completed NCT02196233 - Surgical Treatment of Adult Trigger Finger
Terminated NCT05082480 - Evaluate the Effectiveness of Crosslinked HA on the Adhesion Preventing After Trigger Finger Release Surgery N/A
Recruiting NCT05045157 - Effectiveness of Percutaneous Pulley Release With Infiltration, Versus Infiltration Alone in Trigger Finders N/A
Active, not recruiting NCT01886157 - Treatment of Trigger Finger With Steroid Injection Versus Steroid Injection and Splinting N/A
Recruiting NCT00951236 - Study Comparing One Versus Two Cortisone Injections for Trigger Finger N/A
Withdrawn NCT04855942 - Focused Extracorporeal Shock Wave Therapy (ESWT) Versus Traditional Physiotherapy in the Treatment of Trigger Finger N/A