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NCT02087228 · ClinicalTrials.gov registry record · NA
Evaluation of the Endometrial Cavity After Endometrial Ablation
A NA study, sponsored by Baylor Research Institute.
- Terminated
- Registry status
- NA
- Development phase
- 25
- Enrollment target
NCT02087228 is a NA study that was terminated before completion, run by Baylor Research Institute. The registered enrollment target is 25 participants.
The verdict
NCT02087228, a NA study, was terminated before completion, sponsored by Baylor Research Institute.
- TERMINATED
- Registry status
- NA
- Development phase
- 25 participants
- Enrollment target
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.
Interventions
- DEVICE Genesys HydroTherm Ablator
- DEVICE radiofrequency energy ablation device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 25 participants |
| Start Date | 2013-09 |
| Est. Completion | 2015-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02087228
The ClinicalTrials.gov registry entry for NCT02087228 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Baylor Research Institute, which has 180 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Genesys HydroTherm Ablator is the first listed.
NCT02087228 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02087228 about?
NCT02087228 is a clinical study titled "Evaluation of the Endometrial Cavity After Endometrial Ablation". 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 perf...
What is the current status of trial NCT02087228?
This trial is currently terminated. It is a NA study. The enrollment target is 25 participants. The study started on 2013-09. Estimated completion is 2015-07.
What interventions are being tested in trial NCT02087228?
The interventions under investigation include: Genesys HydroTherm Ablator (DEVICE), radiofrequency energy ablation device (DEVICE).
Who is sponsoring clinical trial NCT02087228?
This trial is sponsored by Baylor Research Institute, which has 180 total clinical trials registered on ClinicalTrials.gov.
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