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NCT01769131 · ClinicalTrials.gov registry record
A Comparison of Two Instruments for Stabilization of the Cervix During Office Procedures
A clinical trial, sponsored by Carilion Clinic.
- Completed
- Registry status
- 81
- Enrollment target
NCT01769131: Completed study, sponsored by Carilion Clinic.
NCT01769131 is a clinical trial that has completed, run by Carilion Clinic. The registered enrollment target is 81 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01769131 has completed, sponsored by Carilion Clinic.
- COMPLETED
- Registry status
- 81 participants
- Enrollment target
Study Summary
An Allis clamp causes less pain and bleeding than a single tooth tenaculum when used for mobilization of the cervix during common gynecologic office procedures. The primary object is to determine the presence of a difference in pain perception between the two instruments. The secondary objective is to evaluate the differences in the frequency of bleeding, that requires treatment, after removal of the instrument and the need to use an alternative instruments.
Primary Outcome
Primary - to determine the presence of a difference in pain perception between the two instruments.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 81 participants |
| Start Date | 2012-09 |
| Est. Completion | 2014-12 |
What the finished NCT01769131 record still lists
NCT01769131 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 81 participants, a relatively small participant target.
The record links to 0 conditions, and to 0 interventions.
NCT01769131 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01769131 about?
NCT01769131 is a clinical study titled "A Comparison of Two Instruments for Stabilization of the Cervix During Office Procedures". An Allis clamp causes less pain and bleeding than a single tooth tenaculum when used for mobilization of the cervix during common gynecologic office procedures. The primary object is to determine the presence of a difference in pain perception between the two instruments. The secondary objective i...
What is the current status of trial NCT01769131?
This trial is currently completed. The enrollment target is 81 participants. The study started on 2012-09. Estimated completion is 2014-12.
Who is sponsoring clinical trial NCT01769131?
This trial is sponsored by Carilion Clinic, which has 45 total clinical trials registered on ClinicalTrials.gov.
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