Actively Recruiting
The Use of Cannabidiol Suppositories for Sexual Pain
Led by London Metropolitan University · Updated on 2026-01-26
50
Participants Needed
1
Research Sites
28 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Research aim: To determine how cannabidiol suppositories might reduce sexual pain during intimacy. Outcomes are also hoped to increase sexual functioning, well-being, and quality of life. Research intention: If cannabidiol suppository intervention reduces sexual pain and increases general well-being, then this research would be repeated on a larger scale, targeting psychosexual services. A brief overview of the intervention: Quantitatively, randomisation of cannabidiol suppositories will be into dose-specific groups. The intervention will be delivered over a period of one month, with follow-up scheduled at 12 weeks. Qualitatively, participants were asked approximately eight open-ended feedback questions throughout the study.
CONDITIONS
Official Title
The Use of Cannabidiol Suppositories for Sexual Pain
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Has previously used cannabidiol in any form without allergic reaction
- Is currently experiencing sexual pain
- Does not have other co-occurring difficulties
- Has attempted sexual intercourse in the last month
- Is 18 years old or older
- Can read and write English
- Has mild symptoms on Patient Health Questionnaire 9 (score 0-9)
- Has mild symptoms on General Anxiety Disorder 7 screening (score 0-9)
- No restrictions on sex, gender, sexuality, or disability
You will not qualify if you...
- Has experienced an allergic reaction to cannabidiol in any form
- Has not attempted sexual intercourse in the last month
- Has co-occurring difficulties
- Is younger than 18 years old
- Is not experiencing sexual pain
- Has moderate to severe symptoms on Patient Health Questionnaire 9 (score 10-27)
- Has moderate to severe symptoms on General Anxiety Disorder 7 screening (score 10-21)
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
School of Social Sciences and Professions
London, United Kingdom, N7 8DB
Actively Recruiting
Research Team
A
Anna Kamyk
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
4
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