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Impact of subcuticular absorbable continuous suture compared with interrupted transcutaneous silk/nylon suture on wound healing in laparoscopic colorectal cancer surgery: a prospective randomized controlled clinical trial

Impact of subcuticular absorbable continuous suture compared with interrupted transcutaneous silk/nylon suture on wound healing in laparoscopic colorectal cancer surgery: a prospective randomized controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053391
Enrollment
Unknown
Registered
2021-11-20
Start date
2021-12-01
Completion date
Unknown
Last updated
2022-09-26

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

Conditions

Colorectal cancer and SSI

Interventions

Experimental group:subcuticular absorbable continuous suture
Control group:interrupted transcutaneous silk/nylon suture

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: All patients planed to undergo elective laparoscopic assisted radical resection of colorectal cancer.

Exclusion criteria

Exclusion criteria: 1. Emergency surgery; 2. Hemoglobin = 4.

Design outcomes

Primary

MeasureTime frame
The incidence of superficial Surgical Site Infection;—

Secondary

MeasureTime frame
pain level;Healing speed;Cosmetic effect;—

Countries

China

Contacts

Public ContactYang Lie

West China Hospital of Sichuan University

lie_222@163.com+86 18980602267

Outcome results

None listed

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