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Effect of Topical Trimebutine on Pain After Hemorrhoidectomy

Effect of Trimebutine on Postoperative Pain After Milligan-Morgan Hemorrhoidectomy: A Randomized Controlled Trial

Status
Suspended
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03036111
Enrollment
42
Registered
2017-01-30
Start date
2017-02-01
Completion date
2018-04-01
Last updated
2017-08-29

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

Conditions

Hemorrhoids

Brief summary

Trimebutine acts through smooth muscle relaxation. It is presumed that the topical application of trimebutine after hemorrhoidectomy may help relieve pain after the procedure by relaxing the internal anal sphincter spasm.

Detailed description

A randomized trial will be carried out to investigate the effect of trimebutine on pain after Milligan-Morgan hemorrhoidectomy. Trimebutine relaxes the internal anal sphincter spasm which usually occurs after excisional hemorrhoidectomy.

Interventions

Trimebutine suppository will be inserted in the anal canal on completion of hemorrhoidectomy then at six and 12 hours postoperatively.

PROCEDUREHemorrhoidectomy

Patients will undergo classic Milliagn-Morgan hemorrhoidectomy

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients of both genders aging between 18-70 years with grade III/VI internal hemorrhoids will be included

Exclusion criteria

* Patients with grade I/II internal hemorrhoids or external hemorrhoids. * Patients with associated anorectal pathology such as anal fissure, anal fistula, rectal prolapse, neoplasm, solitary rectal ulcer, and inflammatory bowel diseases.\\ * Patients with recurrent hemorrhoids after previous surgery.

Design outcomes

Primary

MeasureTime frameDescription
Pain assessment assessed using visual analogue score from 0-10Pain will be assessed at 12 hours after the procedureAnal pain will be assessed using visual analogue score from 0-10

Countries

Egypt

Outcome results

None listed

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