Percutaneous trigger finger release, Probe Knife compared with 18-guage needle : A randomized control trial

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

TCTR

Registry ID

TCTR20140529001

Enrollment

128

Registered

2014-05-29

Start date

2014-05-30

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 Percutaneous tenolysis percutaneous release

Interventions

Percutaneous tenolysis,Percutaneous tenolysis

Active Comparator Procedure/Surgery,Active Comparator Procedure/Surgery

Needle group,Probe scalpel

Eligibility

Sex/Gender

All

Age

30 Years to 80 Years

Inclusion criteria

Inclusion criteria: Painful triggering finger Locking finger

Exclusion criteria

Exclusion criteria: Previous hand disease and hand injury

Design outcomes

Primary

Measure	Time frame
Post operative pain VAS	—

Secondary

Measure	Time frame
operative time, time return to work, adverse events, paient satisfaction, pinch strength questionaire, tip pinch guage	—

Countries

Thailand

Contacts

Public ContactSittichoke Anuntaseree

asittich@medicine.psu.ac.th66869691017

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026

Percutaneous trigger finger release&#44; Probe Knife compared with 18&#45;guage needle : A randomized control trial