Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
All Genders
Healthy Volunteers
NCT07271030

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

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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

Age: 18Years - 100Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

School of Social Sciences and Professions

London, United Kingdom, N7 8DB

Actively Recruiting

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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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