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Comparing Patient-Centered Outcomes After Treatment for Uterine Fibroids

NCT02819609 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 12234

Last updated 2016-06-30

No results posted yet for this study

Summary

The purpose of this observational, retrospective database study of patients with uterine fibroids is to compare the durability of symptom relief after uterus-conserving treatments for symptomatic fibroids in terms of incidence of, and time to, new or recurrent symptoms and subsequent procedures and evaluate the effect stakeholder participation had on the research process.

Conditions

  • Uterine Fibroids

Interventions

PROCEDURE

myomectomy

Myomectomy as part of routine clinical care

PROCEDURE

endometrial ablation

Endometrial ablation as part of routine clinical care

PROCEDURE

uterine artery embolization

Uterine artery embolization as part of routine clinical care

PROCEDURE

MRI-guided focused ultrasound ablation

MRI-guided focused ultrasound ablation as part of routine clinical care

Sponsors & Collaborators

  • Center for Medical Technology Policy

    collaborator UNKNOWN

  • Duke University

    collaborator OTHER

  • Quintiles, Inc.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
54 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-11-30
Primary Completion
2015-01-31
Completion
2015-01-31

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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 NCT02819609 on ClinicalTrials.gov