Study of Postoperative Analgesia in Bunionectomy

Pacira

Status and phase

Completed

Phase 3

Conditions

Hallux Valgus

Bunion

Treatments

Drug: Placebo

Drug: SKY0402

Study type

Interventional

Funder types

Industry

Identifiers

NCT00890682

SKY0402C317

Details and patient eligibility

About

After undergoing bunion surgery, patients are given a pain medicine injection that may last for up to several days or a placebo. Their pain and pain medicine use is then monitored.

Full description

Following drug study administration, safety and efficacy assessments were conducted

Enrollment

193 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age ≥ 18 years at the Screening visit
Scheduled to undergo primary unilateral first metatarsal osteotomy without hammertoe
Female subjects must be surgically sterile or at least two years menopausal, or using an acceptable method of birth control. If of childbearing potential, have a documented negative blood or urine pregnancy test within 24 hours before surgery
Clinical laboratory values less than or equal to twice the upper limit of normal or, if abnormal, deemed not clinically significant per the Investigator
Ability to provide informed consent, adhere to the study visit schedule and complete all study assessments

Exclusion criteria

Currently pregnant, nursing, or planning to become pregnant during the study or within one month after study drug administration
Chronic user of analgesic medications, including taking opioid medications for more than 14 days in the last 3 months, or non-opioid pain medications more than 5 times per week
Use of any non-steroidal anti-inflammatory drug (NSAID) including selective COX-2 inhibitor within three days of surgery
Use of acetaminophen within 24 hours of surgery
Use of selective serotonin reuptake inhibitors (SSRIs), gabapentin, pregabalin (Lyrica), duloxetine (Cymbalta) within three days of surgery
Current use of systemic glucocorticosteroids or use of systemic glucocorticoids within one month of enrollment into this study
Peripheral neuropathy including diabetic neuropathy, chemotherapy-induced neuropathy, HIV neuropathy
History of hepatitis
History of, suspected, or known addiction to or abuse of drugs or alcohol within the past two years
Failure to pass urine drug screen
Current evidence of alcohol abuse (greater than 4 units of alcohol per day: 1 unit = ½ pint of beer, 1 glass of wine or 1 oz. of spirits)
Evidence of peripheral ischemic disease
Type I or Type II diabetes
Current acute or chronic medical or major psychiatric disease that, in the opinion of the Investigator, would interfere with the evaluation of study drug efficacy or safety
Malignancy in the last 2 years, with the exception of non-metastatic basal cell or squamous cell carcinoma of the skin or localized carcinoma in situ of the cervix
Administration of an investigational drug within 30 days prior to study drug administration, or planned administration of another investigational product or procedure during the subject's participation in this study
Previous participation in a SKY0402 study
Significant medical conditions or laboratory results that, in the opinion of the Investigator, indicate an increased vulnerability to study drugs and procedures
Current painful physical conditions or concurrent surgery other than bunionectomy that may require analgesic treatment (such as NSAID or opioid) in the postoperative period for pain that is not strictly related to the bunionectomy procedure and may confound the postoperative assessments