CompletedPhase 1/2

Permanent Occlusion of Uteine Arteies in Management of Abnormal Uterine Bleeding

Egypt116 participantsStarted 2011-10

Plain-language summary

Prospective observational interventional study , The study done in two phases: 1. Phase one from October 2011to May 2012 pilot study including twenty nine (29) premenopausal patients followed up for six months 2. Phase two from October 2012 till May 2014. Including Eighty nine (89) premenopausal patients all of them needing to preserve their uteri.

Who can participate

Age range34 Years – 45 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * premenopausal with abnormal uterine bleeding and completed their families having normal endometrium (biopsy in preceding 6 months ) and may have uterine intramural myomas not exceeding 150 ml in volume and away from uterine cavity by at least 1cm and /or adenomyosis Exclusion Criteria: * patients wishing future fertility * endometrial sampling not done or more than 6 months or myoma encroaching or distorting cavity or larger than 150 ml in volume

What they're measuring

uterine bleeding

Timeframe: October 2011 till January 2016

Trial details

NCT IDNCT05423067

SponsorMansoura Integrated Fertility Center

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2012-10

View on ClinicalTrials.gov More Other Abnormal Uterine and Vaginal Bleeding trials