sefulness of perianal surgical skin preparation before hemorrhoidectomy - a randomized, controlled, clinical trial

Not Applicable

• Conditions: K64.1; K64.2; Second degree haemorrhoids; Third degree haemorrhoids

• Registration Number: DRKS00032524
• Lead Sponsor: Evangelisches Krankenhaus Lippstadt gGmbH

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-07-29
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

Planned Milligan-Morgan haemorrhoidectomy for second- or third-degree hemorrhoids

Exclusion Criteria

Immunosuppression, septic focus, pregnancy, lack of informed consent

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Surgical site infection (according to CDC criteria) or delayed wound healing (< 50% granulation tissue after 14 days)

Secondary Outcome Measures

Name	Time	Method
postoperative pain (day 1, 2, 7, 28), length of hospital stay, adverse events (according to Clavien-Dindo classification), patient satisfaction