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Suture vs Staples for Skin Closure After Liver Resection

A Randomised Controlled Trial to Compare Subcuticular Suture vs Staples for Skin Closure After Liver Resection.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02046239
Enrollment
200
Registered
2014-01-27
Start date
2013-03-01
Completion date
2015-01-01
Last updated
2019-07-08

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

Conditions

Closure of the Skin After Liver Resection

Brief summary

Closure of the skin after liver resection (surgery to remove part of the liver) may be achieved by one of several methods. The standard method at our institution is to use stainless steel staples to adjoin the two sides of skin. Alternatively, a continuous absorbable suture may be used to sew the skin together. The ideal method of closure should be safe, effective, associated with minimal patient discomfort and have a good cosmetic result. At present, there is no scientific evidence to describe which method is most suitable following liver resection. The primary aims of this study is to investigate which method (subcuticular sutures vs staples) offers the best result in postoperative rate of (1) skin infection, (2) skin dehiscience (separation of skin) and (3) time taken to perform skin closure. In addition, we are interested in which method is best for patient satisfaction and cosmetic appearance and which method is most cost effective.

Interventions

PROCEDURESuture Group
BIOLOGICALStaple Group (control)

Sponsors

The Leeds Teaching Hospitals NHS Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients undergoing liver resection surgery for benign or malignant aetiology * All patients undergoing surgery as a living liver donor.

Exclusion criteria

* Any patient with an active wound infection * Any patient with an active incisional wound hernia from previous surgery * Synchronous bowel/liver surgery * History of keloid formation

Design outcomes

Primary

MeasureTime frame
Post-operative infection time1 year

Secondary

MeasureTime frame
Time taken for skin closure12 months

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026