Efficacy and Safety of A Collagen Bupivacaine Implant in Patients After Gastrointestinal Surgery

Pain, Postoperative Clinical Trial

Official title:

A Phase II, Randomized, Single-dose, Double-blind, Placebo-controlled Study to Investigate the Efficacy, Safety and Pharmacokinetic Profile of the CollaRx Bupivacaine Implant in Patients After Gastrointestinal Surgery

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00661466
• Other study ID #: INN-CB-004
• Status: Terminated
• Phase: Phase 2
• Start date: July 24, 2008
• Est. completion date: February 10, 2009

Study information

• Verified date: September 2020
• Source: Innocoll
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether the CollaRx Bupivacaine Implant (bupivacaine sponge) is safe and effective in reducing the amount of narcotic pain medication needed to control pain during the first 24 hours after gastrointestinal (GI) surgery.

Description:

Gastrointestinal (GI) surgery encompasses a range of surgical procedures that involve abdominal incision. Gastrointestinal surgery may be performed to treat an abdominal aortic aneurysm, ulcerative colitis, Crohn's disease, gallbladder disease, bile duct disease and morbid obesity. Although less invasive laparoscopic procedures are performed when warranted, open abdominal surgery is required for certain indications and for more complicated or advanced cases.

Bupivacaine is a local anesthetic (pain medicine) that has an established safety profile. Collagen is a protein that is found in all mammals. The CollaRx Bupivacaine implant is a thin flat sponge made out of collagen that comes for cow tendons and contains bupivacaine. When inserted into a surgical site, the collagen breaks down and bupivacaine is released at the site but very little is absorbed into the blood stream. The high levels of bupivacaine at the surgical site may result in less pain for several days after surgery.

This study will compare the amount of narcotic pain medication required after surgery in patients who receive the CollaRx Bupivacaine implant or a plain collagen sponge.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 7
• Est. completion date: February 10, 2009
• Est. primary completion date: January 10, 2009
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Must be a man or woman who is = 18 and = 75 years of age.

• Has a body mass index (BMI) > 19 and < 40 kg/m2.

• Has a planned elective surgery that requires a vertical or transverse abdominal incision (including but not limited to abdominal aortic aneurysm repair, cholecystectomy and simple bowel resection) to be performed according to standard surgical technique under general anesthesia.

• Has a risk classification of I, II or III according to the American Society of Anesthesiologists (ASA)

• If female, is nonpregnant (negative pregnancy test at Screening and Day 0 before surgery) and nonlactating.

• If female, is either not of childbearing potential or practicing a defined medically acceptable method of birth control and agrees to continue with the regimen throughout the study.

• Is free of other physical or mental conditions that, in the opinion of the Investigator, may confound quantification of postoperative pain resulting from the surgery.

• Has the ability and willingness to comply with the study procedures and the use of the pain scales; is deemed capable of operating a PCA device; and is able to communicate meaningfully with the study staff.

• Must voluntarily sign and date an informed consent form (ICF) that is approved by an IRB prior to the conduct of any study specific procedures.

• Must be able to fluently speak and understand English and be able to provide meaningful written informed consent for the study.

Exclusion Criteria:

• Has known hypersensitivity to amide local anesthetics, opioids or bovine products, or to inactive ingredients of the test article.

• Has 1 of the following surgical procedures planned: total abdominal hysterectomy, omentectomy or surgical procedure for staging cancer.

• Requires the use of Seprafilm® or other absorbable adhesion barriers for the GI surgery.

Requires any additional surgical procedures either related or unrelated to the GI surgery during the same hospitalization.

• Is required to receive neuraxial (spinal or epidural) opioid analgesics during the study.

• Has cardiac arrhythmia or atrioventricular (AV) conduction disorders.

• Concomitantly uses antiarrhythmics (eg, amiodarone), propranolol or strong/moderate cytochrome P450 (CYP) 3A4 inhibitors or inducers (eg, macrolide antibiotics and grapefruit juice).

• Has used long acting analgesics within 24 hours of surgery. Short acting analgesics such as acetaminophen may be used on the day of surgery but are subject to preoperative restrictions for oral intake.

• Has used aspirin or aspirin containing products within 7 days of surgery. Aspirin at a dose of = 325 mg is allowed for cardiovascular prophylaxis if the patient has been on a stable dose regimen for = 30 days prior to Screening.

• Has undergone another major surgery within 3 months of the GI surgery.

• Has known or suspected history of alcohol or drug abuse or misuse within 3 years of Screening or evidence of tolerance or physical dependency on opioid analgesics or sedative hypnotic medications.

Related Conditions & MeSH terms

• Pain, Postoperative

Intervention

Drug:
• Bupivacaine Collagen Sponge

• Placebo
placebo

Locations

Country	Name	City	State
United States	Albany Medical Center Hospital	Albany	New York

Sponsors (2)

Lead Sponsor	Collaborator
Innocoll	Premier Research Group plc

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The Total Amount of Opioid Rescue Analgesia Used	Study Terminated early due to very poor study enrollment. Target recruitment not met. Primary outcome not measured - planned statistical analyses was not performed.	0 to 24 hours postoperatively
Secondary	The Total Amount of Opioid Rescue Analgesia Used	Study Terminated Early - Secondary end point not measured - not done - Study Terminated early due to very poor study enrollment. Target recruitment not met. Primary outcome not measured - planned statistical analyses was not performed.	0 to 48 hours postoperatively
Secondary	The Total Amount of Opioid Rescue Analgesia Used	Study Terminated Early - Secondary end point not measured - not done - Study Terminated early due to very poor study enrollment. Target recruitment not met. Primary outcome not measured - planned statistical analyses was not performed.	0 to 72 hours postoperatively
Secondary	Pain Intensity Rating on the Visual Analogue Scale (VAS)	Study Terminated Early - Secondary end point not measured - not done - Study Terminated early due to very poor study enrollment. Target recruitment not met. Primary outcome not measured - planned statistical analyses was not performed.	1, 1.5, 2, 3, 4, 5, 6, 24, 48 and 72 hours after Time 0
Secondary	Pain Intensity Rating on a 4-point Scale	Study Terminated Early - Secondary end point not measured - not done	At 1, 1.5, 2, 3, 6, 9, 12, 18, 24, 36, 48 and 72 hours postoperatively
Secondary	Pain Relief Rating on a 5-point Scale	Study Terminated Early - Secondary end point not measured - not done - Study Terminated early due to very poor study enrollment. Target recruitment not met. Primary outcome not measured - planned statistical analyses was not performed.	At 30 minutes, 1, 1.5, 2, 3, 4, 5, 6, 24, 48 and 72 hours after Time 0
Secondary	Patient Global Evaluation of Study Treatment on a 5-point Scale	Study Terminated Early - Secondary end point not measured - not done	At 72 hours after time 0
Secondary	Time to First Use of Opioid Rescue Analgesia	Study Terminated Early - Secondary end point not measured - not done - Study Terminated early due to very poor study enrollment. Target recruitment not met. Primary outcome not measured - planned statistical analyses was not performed.	actual time from time 0
Secondary	Pharmacokinetic Parameters	Study Terminated Early - Secondary end point not measured - not done - Study Terminated early due to very poor study enrollment. Target recruitment not met. Primary outcome not measured - planned statistical analyses was not performed.	30 minutes, 1, 1.5, 2, 3, 4, 5, 6, 9, 12, 18, 24, 36, 48 and 72 hours postoperatively
Secondary	The Incidence of Treatment-emergent Adverse Events	Study Terminated Early - Secondary end point not measured - not done - Study Terminated early due to very poor study enrollment. Target recruitment not met. Primary outcome not measured - planned statistical analyses was not performed.	Through 30 days after surgery
Secondary	Changes in Vital Sign Measurements	Study Terminated Early - Secondary end point not measured - not done - Study Terminated early due to very poor study enrollment. Target recruitment not met. Primary outcome not measured - planned statistical analyses was not performed.	Through 72 hours post insertion