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Efficacy and Safety of ALGRX 4975 in the Treatment of Postoperative Pain After Gall Bladder Removal

Primary Purpose

Postoperative Pain

Status
Completed
Phase
Phase 2
Locations
Former Serbia and Montenegro
Study Type
Interventional
Intervention
ALGRX 4975
Sponsored by
AlgoRx Pharmaceuticals
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Postoperative Pain focused on measuring Postoperative pain, Open cholecystectomy, Capsaicin

Eligibility Criteria

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

Inclusion Criteria: Subjects undergoing open cholecystectomy with the subcostal approach for cholelithiasis/cholecystitis American Society of Anesthesiologists (ASA) Class I or II Exclusion Criteria: Active pancreatitis, any obstruction of the biliary tree, or hyperbilirubinemia (total bilirubin > 2.5 mg/dL) Previous abdominal surgical procedure with the exception of inguinal hernia repair or appendectomy by the lateral approach or cesarean section or hysterectomy if the surgery was performed more than 1 year prior to study participation and the subject experienced no postoperative complications Diabetes mellitus with HbA1C > 9.5 or a history of prolonged uncontrolled diabetes mellitus Systolic blood pressure greater than 150 mmHg or diastolic greater than 95 mmHg

Sites / Locations

  • Emergency Center, Clinical Center of Serbia

Outcomes

Primary Outcome Measures

Average numeric rating scale (NRS) scores for pain on ambulation assessed in the evening on the day of surgery and the first four postoperative days

Secondary Outcome Measures

Time to first use and total supplemental pain medication use
NRS scores for pain on the first 14 days postoperatively
Spirometry on postoperative days 1 to 4
Safety and tolerability
Pharmacokinetics

Full Information

First Posted
August 18, 2005
Last Updated
December 18, 2006
Sponsor
AlgoRx Pharmaceuticals
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1. Study Identification

Unique Protocol Identification Number
NCT00133133
Brief Title
Efficacy and Safety of ALGRX 4975 in the Treatment of Postoperative Pain After Gall Bladder Removal
Official Title
A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Analgesic Efficacy, Safety and Tolerability of ALGRX 4975 in Subjects After Open Cholecystectomy
Study Type
Interventional

2. Study Status

Record Verification Date
February 2006
Overall Recruitment Status
Completed
Study Start Date
July 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2005 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
AlgoRx Pharmaceuticals

4. Oversight

5. Study Description

Brief Summary
Postoperative pain after gall bladder removal can be significant, mobility limiting and extend hospital stay. ALGRX 4975 is an ultra-pure form of capsaicin, which is a pain medicine that has the potential for long-term pain relief following a single administration. This study will determine whether ALGRX 4975 can provide pain relief following gall bladder removal.
Detailed Description
Postoperative pain after open cholecystectomy can be significant and mobility limiting, causing increased risk of deep venous thrombosis, pulmonary complications, and extended hospital stay. With increasing emphasis on early postoperative mobilization, adequate postoperative pain control is essential. Acute postoperative pain is currently managed largely with opioids and co-administration of nonsteroidal anti-inflammatory drugs (NSAIDS). Opioids are highly effective in managing acute postoperative pain, however dosing is often limited by side effects such as respiratory depression, nausea and vomiting, and sedation. NSAIDS are administered to reduce opioid use, but may also have limiting side effects, such as gastrointestinal toxicity and platelet dysfunction. New strategies to manage acute postoperative pain would provide clinical benefit. ALGRX 4975 is an ultra-pure form of capsaicin, which is a pain medicine that has the potential for long-term pain relief following a single administration. This study will determine whether ALGRX 4975 can provide pain relief following open cholecystectomy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Pain
Keywords
Postoperative pain, Open cholecystectomy, Capsaicin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
40 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
ALGRX 4975
Primary Outcome Measure Information:
Title
Average numeric rating scale (NRS) scores for pain on ambulation assessed in the evening on the day of surgery and the first four postoperative days
Secondary Outcome Measure Information:
Title
Time to first use and total supplemental pain medication use
Title
NRS scores for pain on the first 14 days postoperatively
Title
Spirometry on postoperative days 1 to 4
Title
Safety and tolerability
Title
Pharmacokinetics

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects undergoing open cholecystectomy with the subcostal approach for cholelithiasis/cholecystitis American Society of Anesthesiologists (ASA) Class I or II Exclusion Criteria: Active pancreatitis, any obstruction of the biliary tree, or hyperbilirubinemia (total bilirubin > 2.5 mg/dL) Previous abdominal surgical procedure with the exception of inguinal hernia repair or appendectomy by the lateral approach or cesarean section or hysterectomy if the surgery was performed more than 1 year prior to study participation and the subject experienced no postoperative complications Diabetes mellitus with HbA1C > 9.5 or a history of prolonged uncontrolled diabetes mellitus Systolic blood pressure greater than 150 mmHg or diastolic greater than 95 mmHg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Slobodan Krstic, MD
Organizational Affiliation
Emergency Center, Clinical Center of Serbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Emergency Center, Clinical Center of Serbia
City
Belgrade
ZIP/Postal Code
11000
Country
Former Serbia and Montenegro

12. IPD Sharing Statement

Learn more about this trial

Efficacy and Safety of ALGRX 4975 in the Treatment of Postoperative Pain After Gall Bladder Removal

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