Skip to main content
Clinical Trials/NCT01534416
NCT01534416
Completed
Not Applicable

Use of Paracervical Block in Laparoscopic Gynecologic Surgery: A Randomized Controlled Trial

Icahn School of Medicine at Mount Sinai1 site in 1 country132 target enrollmentSeptember 2011

Overview

Phase
Not Applicable
Intervention
Bupivacaine
Conditions
Postoperative Pain
Sponsor
Icahn School of Medicine at Mount Sinai
Enrollment
132
Locations
1
Primary Endpoint
Number of Participants With Hospital Admission for Postoperative Pain Control
Status
Completed
Last Updated
8 years ago

Overview

Brief 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.

Detailed Description

A variety of traditionally open surgical procedures have recently become minimally invasive through the use of laparoscopic technology. Gynecologic surgeries are no exception. However, some gynecologic laparoscopic procedures are associated with significant post-operative pain, necessitating prolonged hospitalization, use of post-operative opioids, and in some cases, the development of chronic post-operative pain. Prolonged hospitalization and use of opioids pose important patient safety concerns, such as increased risk of hospital borne illnesses and medication errors; in addition, opioids may cause respiratory depression and addiction. Given the rising cost of health care there is also an economic incentive to eliminate the need for hospital admission due to post-operative pain. Preemptive analgesia involves nerve blockade or administration of pain medication systemically prior to incision to reduce post-procedure pain. Paracervical blockade is a form of preemptive analgesia. Paracervical blocks have been demonstrated to be safe and effective for obstetrical procedures in reducing post-operative pain since the 1970s. Recently they have also been shown to be efficacious for reducing post-operative pain in vaginal hysterectomy (Long et al, Int Urogynecol J (2009) 20:5-10). For the present investigation, we intend to study the effectiveness of paracervical blockade for laparoscopic and robotic-assisted laparoscopic gynecological surgery. We hypothesize that paracervical blockade prior to surgical incision will lessen levels of post-operative pain, reduce use of opioids, and decrease the number of patients requiring hospitalization for pain control. We also hypothesize that the effects may be longer lasting than the immediate post-operative period and may decrease the amount of time to return to normal activity after surgery. Using anecdotal evidence from the primary investigator, Dr. Ascher-Walsh the rate of hospitalization for laparoscopic hysterectomy (laparoscopic-assisted vaginal hysterectomy, total laparoscopic hysterectomy, laparoscopic assisted supracervical hysterectomy) is approximately 67%. In this study, we wish to decrease hospitalization with the paracervical block by 50%, thus obtaining an overall post-operative hospitalization rate of 33%. For robotic-assisted laparoscopic myomectomy, the rate of hospitalization is 50%. We wish to decrease this by 50% as well. Overall we are aiming to achieve a rate of 30% for post-operative hospitalization for pain control for laparoscopic hysterectomies and robotic myomectomies combined.

Registry
clinicaltrials.gov
Start Date
September 2011
End Date
September 2013
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age 18 or older
  • Scheduled for robotic-assisted laparoscopic myomectomy or laparoscopic hysterectomy, including total and supracervical hysterectomy, laparoscopic-assisted vaginal hysterectomy
  • Surgery being performed for benign disease

Exclusion Criteria

  • Women under 18 years old
  • Pregnancy
  • Suspected or known malignant disease
  • Immunocompromised

Arms & Interventions

Bupivacaine

Subjects receive paracervical block with bupivacaine-epinephrine

Intervention: Bupivacaine

Saline

Subjects receive paracervical injection of normal saline

Intervention: Normal Saline

Outcomes

Primary Outcomes

Number of Participants With Hospital Admission for Postoperative Pain Control

Time Frame: Four hours after conclusion of surgery

Unplanned hospital admissions and the hospital admissions at the request of the patients for pain management

Secondary Outcomes

  • Postoperative Day Pain Medication Use(Postoperative days 0-10)
  • Postoperative Pain Score(1, 2, 4 hour postoperatively, Day 1 post operatively, Day 2 postoperative)

Study Sites (1)

Loading locations...

Similar Trials