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NCT01062087 · ClinicalTrials.gov registry record
Pain Perception After Tubal Ligation
A clinical trial, sponsored by Oklahoma State University Center for Health Sciences.
- Completed
- Registry status
- 62
- Enrollment target
NCT01062087 is a clinical trial that has completed, run by Oklahoma State University Center for Health Sciences. The registered enrollment target is 62 participants.
The verdict
NCT01062087 has completed, sponsored by Oklahoma State University Center for Health Sciences.
- COMPLETED
- Registry status
- 62 participants
- Enrollment target
Study Summary
The purpose of this study is to attempt to determine retrospectively whether there was a statistically significant difference in patient need for postoperative narcotics between two different groups of women who received a laparoscopic tubal ligation. One group received a local anesthetic injection or gel at the surgical sites, in addition to general anesthesia. The other group did not receive any local anesthetic but did receive general anesthesia. The investigators hypothesize that the group that received the local anesthetic injection or gel had lower average postoperative narcotic requirements and shorter postoperative dismissal to home times than the group that did not receive the auxiliary local anesthetic.
Interventions
- DRUG Bupivacaine, Lidocaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 62 participants |
| Start Date | 2010-01 |
| Est. Completion | 2010-12 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01062087
The ClinicalTrials.gov registry entry for NCT01062087 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 62 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Oklahoma State University Center for Health Sciences, which has 24 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Bupivacaine, Lidocaine is the first listed.
NCT01062087 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01062087 about?
NCT01062087 is a clinical study titled "Pain Perception After Tubal Ligation". The purpose of this study is to attempt to determine retrospectively whether there was a statistically significant difference in patient need for postoperative narcotics between two different groups of women who received a laparoscopic tubal ligation. One group received a local anesthetic injection ...
What is the current status of trial NCT01062087?
This trial is currently completed. The enrollment target is 62 participants. The study started on 2010-01. Estimated completion is 2010-12.
What interventions are being tested in trial NCT01062087?
The interventions under investigation include: Bupivacaine, Lidocaine (DRUG).
Who is sponsoring clinical trial NCT01062087?
This trial is sponsored by Oklahoma State University Center for Health Sciences, which has 24 total clinical trials registered on ClinicalTrials.gov.
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