Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
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 is a clinical trial that has completed, run by Carilion Clinic. The registered enrollment target is 81 participants.
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.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 81 participants |
| Start Date | 2012-09 |
| Est. Completion | 2014-12 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01769131
The ClinicalTrials.gov registry entry for NCT01769131 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 81 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Carilion Clinic, which has 45 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 0 interventions.
NCT01769131 reports 0 study locations.
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.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.