The effect of trigger cut on the release of trigger finger.

Evaluating the effectiveness of trigger cut tool in Pulley A1 release and trigger finger treatment

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20250515065744N1

Enrollment

Registered

2025-06-06

Start date

2025-06-20

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

Trigger finger. Trigger finger

Interventions

Intervention group: Intervention group: Patients with trigger finger visiting Hazrat Fatemeh Educational and Therapeutic Center in the year 1404 (2025-2026) will be treated using the cut trigger tool.

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: • Clinical diagnosis of the disease

Exclusion criteria

Exclusion criteria: • Age under 18 years of patients • Presence of trigger finger condition due to underlying causes such as diabetes and rheumatoid arthritis • Use of similar treatment methods on the finger under current study within the past three months

Design outcomes

Primary

Measure	Time frame
Frequency rate of trigger finger stages. Timepoint: Before, three weeks after, and six weeks after the surgery. Method of measurement: Count.;Mean pain during flexion. Timepoint: Before, three weeks after, and six weeks after the surgery. Method of measurement: VAS scale.;Mean pain during passive extension. Timepoint: Before, three weeks after, and six weeks after the surgery. Method of measurement: VAS scale.;Frequency of tenderness occurrence. Timepoint: three weeks after, and six weeks after the surgery. Method of measurement: Checklist.;Complications of paresthesia and pain at the pulley site. Timepoint: three weeks after, and six weeks after the surgery. Method of measurement: Checklist.	—

Measure

Time frame

Frequency rate of trigger finger stages. Timepoint: Before, three weeks after, and six weeks after the surgery. Method of measurement: Count.;Mean pain during flexion. Timepoint: Before, three weeks after, and six weeks after the surgery. Method of measurement: VAS scale.;Mean pain during passive extension. Timepoint: Before, three weeks after, and six weeks after the surgery. Method of measurement: VAS scale.;Frequency of tenderness occurrence. Timepoint: three weeks after, and six weeks after the surgery. Method of measurement: Checklist.;Complications of paresthesia and pain at the pulley site. Timepoint: three weeks after, and six weeks after the surgery. Method of measurement: Checklist.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Akbari

Iran University of Medical Sciences

hakbari1339@yahoo.com+98 21 8871 7272

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026