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Topical Versus Oral Metronidazole Following Excisional Haemorrhoidectomy

Primary Purpose

Hemorrhoids, Postoperative Pain

Status
Completed
Phase
Phase 4
Locations
New Zealand
Study Type
Interventional
Intervention
Metronidazole Oral
Metronidazole Ointment
Placebo Oral Tablet
Placebo Ointment
Sponsored by
University of Auckland, New Zealand
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemorrhoids focused on measuring Hemorrhoidectomy, Metronidazole, Postoperative analgesia

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients undergoing excisional haemorrhoidectomy

Exclusion Criteria:

  • < 16 years of age
  • Have a simultaneous operation other than excisional haemorrhoidectomy
  • History of chronic pain
  • Previous allergy/adverse reaction to metronidazole
  • Patients unable to consent or complete data questionnaires due to cognitive impairment

Sites / Locations

  • Manukau SuperClinic, Counties Manukau District Health Board
  • Ormiston Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Group A - Oral

Group B - Topical

Arm Description

Oral metronidazole 400mg 3 times a day for 7 days Placebo ointment applied 3 time times a day for 7 days to affected region

Topical metronidazole ointment 10% 3 times a day for 7 days Oral placebo tablets 3 times a day for 7 days

Outcomes

Primary Outcome Measures

Daily Post-Operative Pain
Daily Post-Operative Pain Measured on Visual Analogue Scale (0 to 10)

Secondary Outcome Measures

Total Analgesia Use
Measured in Morphine Equivalent Doses
Complication Rates
Short term complication rates including adverse reactions, bleeding, paraesthesiae, urinary retention, readmission
Return to Normal Activity
Time to return back to normal activity
Return of Bowel Function
Time for first bowel motion

Full Information

First Posted
November 5, 2017
Last Updated
November 2, 2020
Sponsor
University of Auckland, New Zealand
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1. Study Identification

Unique Protocol Identification Number
NCT03343509
Brief Title
Topical Versus Oral Metronidazole Following Excisional Haemorrhoidectomy
Official Title
A Prospective, Multicentre, Double-Blinded Randomised Controlled Trial Comparing Topical Versus Oral Metronidazole in Reducing Post-Operative Pain Following Excisional Haemorrhoidectomy
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
March 11, 2019 (Actual)
Primary Completion Date
February 1, 2020 (Actual)
Study Completion Date
February 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Auckland, New Zealand

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study aims to determine if topical metronidazole reduces pain more than oral metronidazole following excisional haemorrhoidectomy. The trial will be a multi-centered, patient and investigator blinded superiority trial with two parallel groups and a primary outcome of pain scores during 14 days after surgery. Group A will receive oral metronidazole and placebo cream. Group B will receive placebo tablets and topical metronidazole cream.
Detailed Description
The pathogenesis of post-operative excisional haemorrhoidectomy pain is multi-factorial with secondary bacterial colonisation, inflammation and anal sphincter spasm/hypertonicity all purposed to play a role. Several pharmacological agents have been introduced in the last two decades targeting specific parts of the hypothesized pathway of pain pathogenesis showing promising improvements. Metronidazole is part of the nitroimidazole class of antibiotics and primarily affects anaerobic bacteria and protozoa and traditionally has been used in surgical prophylaxis and treating anaerobic infections. It has been postulated to decrease pain following EH via two mechanisms; first by decreasing secondary bacterial colonisation and hence reducing post-operative inflammation; and second via a hitherto poorly understood direct anti-inflammatory response. The oral route has been initially investigated but topical administration has more recently been mooted for analgesia and theoretically reduces the unpleasant systemic side effects of oral administration. Our research group has recently completed a systematic review of both oral and topical administration of metronidazole. This review showed benefit in reducing postoperative haemorrhoidectomy pain from both routes of administration but this far there has been no comparison of the two routes. Metronidazole has been proposed to have both anti-bacterial and pleiotropic anti-inflammatory properties but its precise mechanism of action is unknown. The increased understanding of this novel use of an agent with a known pharmacological profile will generally broaden our use of a simple, cheap and widespread agent. The investigators hope research into this drug will enable its use beyond that of haemorrhoidectomies, with possible pleiotropic applications into other similar operations. Given the high prevalence of haemorrhoids in a vital segment of New Zealand's population, this research will contribute to improved outcomes for affected patients. Decreasing the significant post-operative pain will improve the quality of life for New Zealanders as well as affected populations worldwide. Socially and financially, it will enable earlier return to normal activity and reduce the burden on visits and readmissions to primary and secondary care, respectively.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemorrhoids, Postoperative Pain
Keywords
Hemorrhoidectomy, Metronidazole, Postoperative analgesia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group A - Oral
Arm Type
Experimental
Arm Description
Oral metronidazole 400mg 3 times a day for 7 days Placebo ointment applied 3 time times a day for 7 days to affected region
Arm Title
Group B - Topical
Arm Type
Experimental
Arm Description
Topical metronidazole ointment 10% 3 times a day for 7 days Oral placebo tablets 3 times a day for 7 days
Intervention Type
Drug
Intervention Name(s)
Metronidazole Oral
Intervention Description
Oral Metronidazole
Intervention Type
Drug
Intervention Name(s)
Metronidazole Ointment
Intervention Description
Metronidazole Ointment
Intervention Type
Drug
Intervention Name(s)
Placebo Oral Tablet
Intervention Description
Placebo Tablet
Intervention Type
Drug
Intervention Name(s)
Placebo Ointment
Intervention Description
Placebo Ointment
Primary Outcome Measure Information:
Title
Daily Post-Operative Pain
Description
Daily Post-Operative Pain Measured on Visual Analogue Scale (0 to 10)
Time Frame
Day 7
Secondary Outcome Measure Information:
Title
Total Analgesia Use
Description
Measured in Morphine Equivalent Doses
Time Frame
Day 7
Title
Complication Rates
Description
Short term complication rates including adverse reactions, bleeding, paraesthesiae, urinary retention, readmission
Time Frame
Day 30
Title
Return to Normal Activity
Description
Time to return back to normal activity
Time Frame
Day 30 (Followed up until returned back to normal)
Title
Return of Bowel Function
Description
Time for first bowel motion
Time Frame
Day 7

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients undergoing excisional haemorrhoidectomy Exclusion Criteria: < 16 years of age Have a simultaneous operation other than excisional haemorrhoidectomy History of chronic pain Previous allergy/adverse reaction to metronidazole Patients unable to consent or complete data questionnaires due to cognitive impairment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrew G Hill, MBChB
Organizational Affiliation
The University of Auckland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Manukau SuperClinic, Counties Manukau District Health Board
City
Auckland
Country
New Zealand
Facility Name
Ormiston Hospital
City
Auckland
Country
New Zealand

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Not to be shared

Learn more about this trial

Topical Versus Oral Metronidazole Following Excisional Haemorrhoidectomy

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