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LigaSure Hemorrhoidectomy Versus Stapled Hemorrhoidopexy

LigaSure Hemorrhoidectomy vs Stapled Hemorrhoidopexy: a Prospective Randomized Clinical Trial

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01097759
Enrollment
115
Registered
2010-04-02
Start date
2006-01-31
Completion date
2008-07-31
Last updated
2010-04-02

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

Conditions

Prolapsed Hemorrhoids

Keywords

hemorrhoids, prolapsed, hemorrhoidectomy, Hemorrhoidopexy, LigaSure, Stapled

Brief summary

This study was designed to compare the outcome of LigaSure hemorrhoidectomy and stapled hemorrhoidopexy for prolapsed hemorrhoids.

Detailed description

The study was designed as a single-blind, prospective, randomized controlled trial and was approved by the Ethics Committee of Ahmadi Hospital, Kuwait. Patients were randomly assigned to undergo either hemorrhoidectomy with the LigaSure device or stapled hemorrhoidopexy. Patients were blinded as to the type of procedure perform. Candidates for the study were consecutive patients with symptomatic grade III or IV hemorrhoids admitted to the Ahmadi Hospital (secondary care hospital), Kuwait, from January 2006 through July 2007.

Interventions

PROCEDURESurgery

Hemorrhoidectomy using the LigaSure sealing device or hemorrhoidopexy using the stapler

Sponsors

Netherlands: Ministry of Health, Welfare and Sports
CollaboratorOTHER_GOV
Kuwait Oil Company Ahmadi Hospital
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Adult (above 18 years) * With prolapsed hemorrhoids (grades III or IV)

Exclusion criteria

* Complicated hemorrhoid * Coexisting perianal disease * Previous perianal surgery * Unfit for general anesthesia * Pregnancy * History of bleeding tendency

Design outcomes

Primary

MeasureTime frameDescription
Assessment of postoperative pain12 monthsPostoperative pain was assessed using the visual analogue scale (VAS)

Secondary

MeasureTime frameDescription
Assessment of postoperative complications12 monthsPostoperative complications and their management were compared between both groups during the followup visits for 12 months

Countries

Kuwait

Outcome results

None listed

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