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Evaluation of the Endometrial Cavity After Endometrial Ablation

NCT02087228 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2016-01-18

No results posted yet for this study

Summary

The purpose of this study is to evaluate the shape, size and appearance of the inside of the uterus six months following an endometrial ablation procedure. Half of the participants will have their ablation performed with a hydrothermal ablation device and the other half will have their ablation performed with a device that uses radiofrequency energy.

Conditions

  • Menorrhagia

Interventions

DEVICE

Genesys HydroTherm Ablator

Heated water is circulated inside the uterus to destroy the lining of the uterus

DEVICE

radiofrequency energy ablation device

Sponsors & Collaborators

  • Baylor Research Institute

    lead OTHER

Principal Investigators

  • Delbert A Johns, M.D. · Texas Health Care, Baylor Research Institute

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2015-07-31
Completion
2015-07-31

Countries

  • United States

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 NCT02087228 on ClinicalTrials.gov