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NCT01534416 · ClinicalTrials.gov registry record · NA
Effect of Paracervical Block on Post Operative Pain in Laparoscopic Gynecologic Surgery
A NA study of Postoperative Pain and Paracervical Block, sponsored by Icahn School of Medicine at Mount Sinai.
- Completed
- Registry status
- NA
- Development phase
- 132
- Enrollment target
- 1
- Study location
NCT01534416 is a NA study of Postoperative Pain and Paracervical Block that has completed, run by Icahn School of Medicine at Mount Sinai. The registered enrollment target is 132 participants, below the 229-participant average among 63 other Postoperative Pain trials with a reported enrollment target (42% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01534416, a NA study of Postoperative Pain and Paracervical Block, has completed, sponsored by Icahn School of Medicine at Mount Sinai.
- COMPLETED
- Registry status
- NA
- Development phase
- 132 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine the effectiveness of placing numbing medication around the cervix prior to performing laparoscopic gynecologic surgery in decreasing pain after surgery. The study focuses on laparoscopic hysterectomies and robotic-assisted myomectomies. It will assess whether patients who receive the medication experience less pain and require less pain medication post operatively and if it helps reduce the number of patients who require hospitalization for pain control following surgery.
Conditions Studied
Interventions
- DRUG Bupivacaine
- DRUG Normal Saline
Study Locations (1)
New York
- Icahn School of Medicine at Mount Sinai - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 132 participants |
| Start Date | 2011-09 |
| Est. Completion | 2013-09 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01534416
The ClinicalTrials.gov registry entry for NCT01534416 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 132 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 229-participant average among 63 other Postoperative Pain trials with a reported enrollment target (42% lower). The listed sponsor is Icahn School of Medicine at Mount Sinai, which has 708 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Postoperative Pain appearing as the primary indexed condition, and to 2 interventions - of which Bupivacaine is the first listed.
NCT01534416 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT01534416 about?
NCT01534416 is a clinical study titled "Effect of Paracervical Block on Post Operative Pain in Laparoscopic Gynecologic Surgery". The purpose of this study is to determine the effectiveness of placing numbing medication around the cervix prior to performing laparoscopic gynecologic surgery in decreasing pain after surgery. The study focuses on laparoscopic hysterectomies and robotic-assisted myomectomies. It will assess whethe...
What is the current status of trial NCT01534416?
This trial is currently completed. It is a NA study. The enrollment target is 132 participants. The study started on 2011-09. Estimated completion is 2013-09.
What conditions does trial NCT01534416 study?
This clinical trial studies the following conditions: Postoperative Pain, Paracervical Block, Laparoscopic Gynecologic Surgery.
What interventions are being tested in trial NCT01534416?
The interventions under investigation include: Bupivacaine (DRUG), Normal Saline (DRUG).
Who is sponsoring clinical trial NCT01534416?
This trial is sponsored by Icahn School of Medicine at Mount Sinai, which has 708 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01534416 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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