A Study to Compare a Newly Developed Suture Material with Standard Sutures for Wound Closure in Patients Undergoing primary skin suturing

A Prospective, Randomized, Parallel-Group Clinical Trial to Evaluate the Safety and Efficacy of a Newly Developed Suture Material Compared to Standard Polyglactin 910 Suture for Wound Closure - GAP -FREE TRIAL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/03/105257

Enrollment

Registered

2026-03-03

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-30

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

Conditions

Health Condition 1: S609- Unspecified superficial injury ofwrist, hand and fingers

Interventions

Intervention1: New Suture Material Group Type - Experimental / Interventional: Patients undergoing primary skin suturing only will receive wound closure using the newly developed suture material. Non

Eligibility

Inclusion criteria

Inclusion criteria: All patients coming to er with laceration

Exclusion criteria

Exclusion criteria: Other softtissue injuries are excluded

Design outcomes

Primary

Measure	Time frame
Prevent wound gapping over the jointsTimepoint: One week /2weeks	—

Secondary

Measure	Time frame
Good healing of the woundTimepoint: One week /2weeks	—

Countries

India

Contacts

Public ContactVidhyaalakshmi S

Saveetha medical college

drgvlapsurg62@gmail.com9842444692

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026