Your session is about to expire
← Back to Search
Anti-infective Agent
Metronidazole for Postoperative Pain in Endometriosis
Phase 4
Recruiting
Led By Resad Pasic, MD, PhD
Research Sponsored by University of Louisville
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Women aged 18-50 years old
Pain score > 2 on a 10 point visual analogue scale at baseline
Must not have
History of Cockayne syndrome
Scheduled hysterectomy
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 5 year postoperatively.
Awards & highlights
Drug Has Already Been Approved
Pivotal Trial
Summary
This trial is testing if taking the antibiotic metronidazole can reduce pain after endometriosis surgery in women aged 18-50. The antibiotic works by killing bacteria to prevent infections, which might help with pain relief.
Who is the study for?
This trial is for women aged 18-50 who can consent, read and write in English or Spanish, have a pain score over 2 due to endometriosis, and are scheduled for excision surgery. It's not for those pregnant, breastfeeding, allergic to metronidazole, with recent endometriosis surgery or certain health issues like abnormal liver tests.
What is being tested?
The study aims to see if low dose oral Metronidazole reduces postoperative pain after endometriosis surgery compared to a placebo. Participants will report their pain levels after receiving either the medication or a placebo.
What are the potential side effects?
Metronidazole may cause side effects such as digestive upset (nausea, vomiting), metallic taste in mouth, dizziness and rash. Alcohol must be avoided as it can lead to severe nausea and vomiting when combined with Metronidazole.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am a woman aged between 18 and 50.
Select...
My pain level is more than 2 out of 10.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have a history of Cockayne syndrome.
Select...
I am scheduled for a hysterectomy.
Select...
I have chosen not to undergo surgery.
Select...
I cannot undergo surgery due to health risks.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 5 years postoperatively
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~5 years postoperatively
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Secondary study objectives
Quality of life scores
Self-reported pain persistence
Sexual health
Other study objectives
Fertility
Awards & Highlights
Drug Has Already Been Approved
The FDA has already approved this drug, and is just seeking more data.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: MetronidazoleExperimental Treatment1 Intervention
Metronidazole
Group II: PlaceboPlacebo Group1 Intervention
Halal and Kosher certified gelatin placebo capsules
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Metronidazole Oral
2019
Completed Phase 4
~190
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for endometriosis include hormonal therapies, anti-inflammatory medications, and antibiotics like metronidazole. Hormonal therapies, such as estrogen-progestin contraceptives and progestins, suppress ovarian function, leading to the atrophy of endometrial tissue and reduced pain.
Anti-inflammatory medications like NSAIDs help alleviate pain by reducing inflammation. Antibiotics like metronidazole disrupt microbial DNA, potentially reducing inflammation and the size of endometriotic lesions.
Understanding these mechanisms helps tailor treatments to individual needs, improving symptom management and quality of life for endometriosis patients.
Antibiotic therapy with metronidazole reduces endometriosis disease progression in mice: a potential role for gut microbiota.New drugs in development for the treatment of endometriosis.[What is new about endometriosis?].
Antibiotic therapy with metronidazole reduces endometriosis disease progression in mice: a potential role for gut microbiota.New drugs in development for the treatment of endometriosis.[What is new about endometriosis?].
Find a Location
Who is running the clinical trial?
University of LouisvilleLead Sponsor
345 Previous Clinical Trials
77,325 Total Patients Enrolled
Resad Pasic, MD, PhDPrincipal Investigator - University of Louisville
University Of Louisville Research Foundation
University Of Louisville School Of Medicine (Medical School)
1 Previous Clinical Trials
142 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have high levels of creatinine in your blood.I had surgery for endometriosis in the last 3 months.I have a history of Cockayne syndrome.I am scheduled for surgery to remove endometriosis.I am scheduled for a hysterectomy.Your liver function test shows results more than two times the normal range.I have chosen not to undergo surgery.I cannot undergo surgery due to health risks.I am a woman aged between 18 and 50.You are allergic to metronidazole.I have not taken Disulfiram in the last 2 weeks.You have passed a screening test called the CAGE questionnaire.My pain level is more than 2 out of 10.You can't stop drinking alcohol while taking the study drug.
Research Study Groups:
This trial has the following groups:- Group 1: Metronidazole
- Group 2: Placebo
Awards:
This trial has 2 awards, including:- Drug Has Already Been Approved - The FDA has already approved this drug, and is just seeking more data.
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Endometriosis Patient Testimony for trial: Trial Name: NCT04554693 — Phase 4
Share this study with friends
Copy Link
Messenger