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CavatermTM vs TCRE in Women With DUB

NCT00549159 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 158

Last updated 2008-05-22

No results posted yet for this study

Summary

The purpose of study is to compare the treatment success in the study groups.

Conditions

  • Dysfunctional Uterine Bleeding

Interventions

DEVICE

Thermal Balloon Endometrial Ablation

Thermal balloon endometrial ablation

DEVICE

Transcervical Resection of the Endometrium

Transcervical resection of the endometrium

Sponsors & Collaborators

  • Pnn Medical A/S

    lead INDUSTRY

Principal Investigators

  • Yanhong Yu, Prof. · Guangzhou Southern Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-10-31
Primary Completion
2009-10-31
Completion
2009-10-31

Countries

  • China

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 NCT00549159 on ClinicalTrials.gov