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Intraperitoneal Aerosolized Delivery of a Local Anesthetic for Post Operative Pain Management. A Double Blind, Randomised Controlled Clinical Trial.

Primary Purpose

Pain, Postoperative, Postoperative Pain, Abdominal Pain

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Intraperitoneal Aerosolization System, IntraMyst
Sponsored by
Northgate Technologies
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pain, Postoperative focused on measuring Laparoscopy, Laparoscopic Surgical Procedures, Laparoscopic Surgery, Gastric Bypass, Drug Delivery Systems, Pain Measurement

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Male or female patients between the ages of 18-65 Patients in general good health requiring elective surgery Exclusion Criteria: Female patients that are pregnant Patients allergic to bupivicaine Patients who have used narcotic drugs within 30 days of the surgical procedure.

Sites / Locations

  • Alexian Brothers Medical Center
  • St. Alexius Medical Center

Outcomes

Primary Outcome Measures

Baseline Pain score before surgery
First Pain score upon arrival in PACU
6 hrs after first recorded pain score
12 hrs after first recorded pain score
24 hrs after first recorded pain score

Secondary Outcome Measures

Full Information

First Posted
February 1, 2006
Last Updated
January 9, 2007
Sponsor
Northgate Technologies
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1. Study Identification

Unique Protocol Identification Number
NCT00286286
Brief Title
Intraperitoneal Aerosolized Delivery of a Local Anesthetic for Post Operative Pain Management. A Double Blind, Randomised Controlled Clinical Trial.
Official Title
Clinical Protocol for the Prospective Double Blind Randomised Controlled Trial for the Use of Intraperitoneal Aerosolized Local Anesthetic
Study Type
Interventional

2. Study Status

Record Verification Date
January 2007
Overall Recruitment Status
Unknown status
Study Start Date
February 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Northgate Technologies

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine the effectiveness of aerosolized pain medication (.5% bupivicaine) delivered into the peritoneal cavity after laparoscopic gastric bypass surgery. This double blind study will include 50 patients. 25 will receive the aerosolized pain medication and 25 will receive a placebo (normal saline). All 50 patients will receive routine/typical methods of post-operative pain management. Post operative pain scores of the patients will be examined to determine the effect of aerosolization.
Detailed Description
Surgical Technique 30 mls of 0.5% bupivacaine with epinephrine standard dose will be distributed into the trocar site wounds after desufflation of the peritoneal cavity. All the patients will be under a consistent intra-abdominal pressure using CO2 and the laparoscopy will be carried out using the same, routine / typical surgical instruments. A. Control Group (n=25): Aerosolized normal saline will be introduced at the end of the procedure, using a specially designed sterile catheter. The catheter will be inserted via trocar port under direct vision. The other end of the catheter will be connected to a 72" Edwards Lifesciences pressure tubing (Ref: 50P172), which will be connected to a B&D 20cc syringe filled with 15 ml of normal saline and inserted into a specially designed syringe pump and pressurizing system designed to aerosolize the specified agent. The total dose of patient delivered normal saline will be 10 ml, with 5 ml remaining contained and undelivered within the catheter and 72" pressure tubing. Routine/Typical methods of post-operative pain management will be employed. B. Aerosolized anesthetic (n=25): at the end of the procedure, the aerosolized local anesthetic will be introduced using a specially designed sterile catheter. The catheter will be inserted via trocar port under direct vision. The other end of the catheter will be connected to a 72" Edwards Lifesciences pressure tubing (Ref: 50P172), which will be connected to a B&D 20cc syringe filled with 15 ml of anesthetic agent and inserted into a specially designed syringe pump and pressurizing system designed to aerosolize the specified agent. The total dose of patient delivered anesthetic will be 10 ml, with 5 ml remaining contained and undelivered within the catheter and 72" pressure tubing. Routine/Typical methods of post-operative pain management will be employed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Postoperative, Postoperative Pain, Abdominal Pain, Obesity, Pneumoperitoneum
Keywords
Laparoscopy, Laparoscopic Surgical Procedures, Laparoscopic Surgery, Gastric Bypass, Drug Delivery Systems, Pain Measurement

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
Double
Allocation
Randomized
Enrollment
50 (false)

8. Arms, Groups, and Interventions

Intervention Type
Device
Intervention Name(s)
Intraperitoneal Aerosolization System, IntraMyst
Primary Outcome Measure Information:
Title
Baseline Pain score before surgery
Title
First Pain score upon arrival in PACU
Title
6 hrs after first recorded pain score
Title
12 hrs after first recorded pain score
Title
24 hrs after first recorded pain score

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female patients between the ages of 18-65 Patients in general good health requiring elective surgery Exclusion Criteria: Female patients that are pregnant Patients allergic to bupivicaine Patients who have used narcotic drugs within 30 days of the surgical procedure.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter C. Rantis Jr., MD
Organizational Affiliation
Alexian Brothers Hospital Network
Official's Role
Principal Investigator
Facility Information:
Facility Name
Alexian Brothers Medical Center
City
Elk Grove Village
State/Province
Illinois
ZIP/Postal Code
60007
Country
United States
Facility Name
St. Alexius Medical Center
City
Hoffman Estates
State/Province
Illinois
ZIP/Postal Code
60194
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Intraperitoneal Aerosolized Delivery of a Local Anesthetic for Post Operative Pain Management. A Double Blind, Randomised Controlled Clinical Trial.

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