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Permanent Occlusion of Uteine Arteies in Management of Abnormal Uterine Bleeding

NCT05423067 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 116

Last updated 2022-06-21

No results posted yet for this study

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.

Conditions

  • Other Abnormal Uterine and Vaginal Bleeding

Interventions

PROCEDURE

bilateral permanent occlusion of uterine arteries

bilateral permanent Occlusion of uterine arteries through abdominal route

Sponsors & Collaborators

  • Mansoura Integrated Fertility Center

    lead OTHER

Principal Investigators

  • Adel S Helal, MD · Mansoura Integrated Fertility Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
34 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-10-31
Primary Completion
2012-10-31
Completion
2015-05-31

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05423067 on ClinicalTrials.gov