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

Sponsor
AlgoRx Pharmaceuticals (Industry)
Overall Status
Completed
CT.gov ID
NCT00133133
Collaborator
(none)
40
1
5
8

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: ALGRX 4975
Phase 2

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.

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double
Primary Purpose:
Treatment
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 Start Date :
Jul 1, 2005
Study Completion Date :
Dec 1, 2005

Outcome Measures

Primary Outcome Measures

  1. 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

  1. Time to first use and total supplemental pain medication use []

  2. NRS scores for pain on the first 14 days postoperatively []

  3. Spirometry on postoperative days 1 to 4 []

  4. Safety and tolerability []

  5. Pharmacokinetics []

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Emergency Center, Clinical Center of Serbia Belgrade Former Serbia and Montenegro 11000

Sponsors and Collaborators

  • AlgoRx Pharmaceuticals

Investigators

  • Principal Investigator: Slobodan Krstic, MD, Emergency Center, Clinical Center of Serbia

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00133133
Other Study ID Numbers:
  • 4975-2-011-2
First Posted:
Aug 22, 2005
Last Update Posted:
Dec 20, 2006
Last Verified:
Feb 1, 2006
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 20, 2006