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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: Completed NA study of Postoperative Pain and Paracervical Block, sponsored by Icahn School of Medicine at Mount Sinai.
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 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (43% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Unplanned hospital admissions and the hospital admissions at the request of the patients for pain management
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 |
What the finished NCT01534416 record still lists
NCT01534416 is an interventional study that assigns participants to a tested intervention. The registered 132 participants enrollment target is mid-sized for trials with a published cap, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (43% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
Similar trials for Postoperative Pain
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT01534416's enrollment target sits among peer trials
132 37th of 120 higher than 84 of 120 other Postoperative Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postoperative Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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