Clin2
NCT05955313Possibly a fitRecruiting

Low-dose naltrexone for different types of vulvodynia pain

VulvodyniaNaltrexoneQuality of Life

Treatments studied

Part of Women’s health & pregnancy clinical trials.

This Phase 2 study tests whether low-dose naltrexone can reduce pain from vulvodynia. It also looks at how well it works across different vulvodynia types, comparing to what participants are already doing for symptoms.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
300 people
Ages
18 years to 50 years
Study type
Interventional

Who can take part

  • You are a woman age 18 up to menopause or up to age 50
  • You are not pregnant and you won’t try to become pregnant for the next 9 months
  • You must sign consent and be generally healthy (WHO score 0–2)
  • You have a diagnosis of vulvodynia and can confirm it at study screening
  • You can’t be taking opioid pain medicines in the last 2 months
  • You must use strong birth control during the study (no abstinence instead)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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