Trial of Extended Release Bupivacaine for Pain Relief After Surgery (PERSIST)

Durect

Status and phase

Completed

Phase 3

Conditions

Post Operative Pain

Treatments

Drug: SABER-Bupivacaine (Part 1)

Drug: Bupivacaine HCl

Drug: Saline Placebo

Drug: SABER-Bupivacaine (Part 2)

Study type

Interventional

Funder types

Industry

Identifiers

NCT02574520

C803-028

Details and patient eligibility

About

This is a research study of SABER® -Bupivacaine, an experimental medication designed to reduce pain for up to 3 days after surgery. Given once by the surgeon at the end of surgery, SABER® - Bupivacaine delivers a locally-acting pain reliever directly to the surgical wound.

The purpose of this study is to measure how well it works in reducing pain after laparoscopic cholecystectomy (surgery to remove the gall bladder) and to investigate the safety of SABER®-Bupivacaine (its side effects).

Enrollment

399 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients scheduled for elective outpatient laparoscopic cholecystectomy using a conventional 4-port laparoscopic procedure.
Must be able and willing to provide written informed consent, complete trial-related procedures, and communicate with the trial staff.
Males and females 18 years of age or older.
ASA Class I, II, or III.
Patients of child-bearing potential must agree to use a medically acceptable method of contraception to prevent pregnancy for the duration of their participation in the trial.
Must be living close enough to the investigative site to attend the four scheduled follow-up clinic visits.

Exclusion criteria

Pregnant or nursing females.
Patients with absolute or relative contraindications to laparoscopic cholecystectomy.
Patients with prior midline abdominal surgery who are at risk for adhesions that may complicate laparoscopic cholecystectomy and/or accurate pain assessments.
Patients requiring emergency surgery or urgent surgery (fewer than 5 days between screening and surgery).
Patients with a pre-planned overnight stay or pre-planned hospital admission.
Patients scheduled for single incision, mini trocars, natural orifice transluminal endoscopic surgery (NOTES), robotic laparoscopic procedures, or any procedure (other than cholangiograms and minimal adhesiolysis) in addition to laparoscopic cholecystectomy.
Patients with known hypersensitivity to amide local anesthetics such as bupivacaine.
Patients with acute pain that is not due to cholecystitis.
Patients with a history of chronic pain unrelated to gallbladder disease.
Patients with ongoing depression or psychosis.
Patients undergoing long-term treatment with opioids or other analgesics, including acetaminophen, NSAIDs, anticonvulsants (gabapentin or pregabalin), and antidepressants (SSRIs, SNRIs, and tricyclics), but not including daily low-dose aspirin.
Patients who are being treated chronically with systemic corticosteroids or who will require peri-operative corticosteroids because of adrenal insufficiency (inhalational or topical corticosteroids are permitted).
Patients who may be unsuitable for opioid administration (such as sensitivity [e.g., history of severe nausea and vomiting] hypersensitivity, known history of abuse or addiction, or unwillingness to take prescribed rescue opioids).
Use of anticoagulants and antiplatelet drugs (with exception of low dose aspirin) in the 1 week prior to surgery.
Patients who are incapable of operating the electronic diary.
Patients participating in any other trial with an investigational drug or device concurrently or less than 30 days prior to surgery for this trial.
Patients who, in the Investigator's opinion, should not participate in the trial or may not be capable of following the trial procedures for any reason.