Comparing Clinical Outcome of nonoperative treatment in A1 pulley trigger finger : Randomized controlled trial

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

TCTR

Registry ID

TCTR20251019005

Enrollment

Registered

2025-10-19

Start date

2025-09-02

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Trigger finger quinnell 1-2 Trigger finger quinnell 1-2

Interventions

rehabilitation by flex the MP joint at 45 degrees for 20 seconds, 30 sessions per day,hand fixed to table + passive flexion of MCP to 45 degrees + Night splint for more than 6 hours

Experimental Other,Experimental Other

isometric stretching,VS Finger stretching + night splint

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Trigger finger quinnell 1-2

Exclusion criteria

Exclusion criteria: Quninnell score above 3

Design outcomes

Primary

Measure	Time frame
Functional hand score/ pain score 3 weeks / 6 weeks/ 3 months QDash score/ Quinnell grading	—

Secondary

Measure	Time frame
Cross-sectional area of the A1 pulley 3 weeks / 6 weeks/ 3 months linear hockey stick ultrasound	—

Countries

Thailand

Contacts

Public Contactyotsaporn ratarat

Vajira Hospital

yotsaporn.rat@nmu.ac.th0923626660

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026