Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06420388

2% Lidocaine Gel in Reducing Postoperative Pain Following Haemorrhoidectomy

Led by E-DA Hospital · Updated on 2024-06-12

400

Participants Needed

1

Research Sites

74 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study is a randomized, double-blind, controlled trial evaluating the efficacy of 2% lidocaine gel in reducing postoperative pain and analgesic consumption after haemorrhoidectomy. 222 patients undergoing Ferguson haemorrhoidectomy will be randomly assigned to receive either 2% lidocaine gel or a non-anaesthetic lubricant gel control. Pain scores using a visual analog scale (VAS) will be assessed at 12 and 24 hours, and 2, 3, and 7 days postoperatively. Analgesic consumption will also be measured.

CONDITIONS

Official Title

2% Lidocaine Gel in Reducing Postoperative Pain Following Haemorrhoidectomy

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosed with Grade III or IV hemorrhoids
  • Candidate for Ferguson haemorrhoidectomy
Not Eligible

You will not qualify if you...

  • Not a candidate for Ferguson haemorrhoidectomy
  • Recurrent hemorrhoidal disease
  • Concurrent anal pathology diagnosed preoperatively, including anal fistula, anal fissure, or anal polyp
  • History of diabetes mellitus
  • History of liver cirrhosis
  • History of inflammatory bowel disease
  • Documented neuropathy
  • Coagulation disorders
  • Currently on anticoagulants
  • Documented allergy to any of the drugs included in the protocol

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

E-Da hospital

Kaohsiung City, Taiwan, 812

Actively Recruiting

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Research Team

C

Chen Chih-i

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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