Moderate to Severe Postoperative Pain Clinical Trial
Official title:
A Randomized, Double-Blind, Multi-Center, Repeat-Dose, Comparison of the Analgesic Efficacy and Safety of Q8003 With Oxycodone and Morphine for the Management of Acute Moderate to Severe Postoperative Pain Following Bunionectomy Surgery
| Verified date | May 2012 |
| Source | QRxPharma Inc. |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Food and Drug Administration |
| Study type | Interventional |
This is a randomized, double-blind, multicenter, fixed dose factorial study of Q8003 12 mg/8 mg versus its individual morphine sulfate and oxycodone hydrochloride components for the management of acute moderate to severe postoperative pain following bunionectomy surgery.
| Status | Completed |
| Enrollment | 522 |
| Est. completion date | March 2010 |
| Est. primary completion date | March 2010 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Patient is male or female and at least 18 years of age. - Females must be non-pregnant, non-lactating, and practicing an acceptable method of birth control, or be surgically sterile or postmenopausal (amenorrhea for = 12 months). Non-pregnancy will be confirmed by pregnancy tests conducted at Screening and Pre-treatment. - Patient is scheduled for bunionectomy surgery, meets the criteria of an ASA Class I to III, and is willing to stay in the study center for at least 48 hours from the initial dose of study medication post surgery. - To be randomized after surgery, the patient must report moderate to severe pain (a score of 2 or more on the 4 point Likert scale or at least 4 on the 11 point NPRS scale). Exclusion Criteria: - In the opinion of the Investigator, has a history of pulmonary, cardiovascular (including uncontrolled hypertension), neurologic, endocrine, hepatic, gastrointestinal, or kidney disease or therapy that, in the opinion of the Investigator, would jeopardize the patient's well being by participation in this study or is mentally or emotionally unsuitable to participate, or unable/unwilling to comply with the study assessments. - Used opiates continuously (including tramadol) for more than ten days in the past year. - Hypersensitivity or poor tolerance to ibuprofen or short term opioids. - Currently receiving any medications that are not at a stable dose (the same dose for > 4 weeks prior to date of surgery). - Was dosed with another investigational drug within 30 days prior to the Screening Visit or has previously received treatment with Q8003. - Current therapy with central nervous system depressant medications that might increase the risks of treatment with opioids (other than those used with surgical anesthesia). - Current evidence of alcohol abuse (regularly drinks more than 4 units of alcohol per day; 1 unit = ½ pint of beer, 1 glass of wine, or 1 ounce of spirit). |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| United States | Investigator Site | Anaheim | California |
| United States | Investigator Site | Owings Mills | Maryland |
| United States | Investigator Site | Pasadena | Maryland |
| United States | Investigator Site | Salt Lake City | Utah |
| United States | Investigator Site | San Antonio | Texas |
| Lead Sponsor | Collaborator |
|---|---|
| QRxPharma Inc. |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Difference in pain intensity scores from baseline | 48 hours | No | |
| Secondary | Safety: adverse events, moderate and severe reports of opioid-related adverse events | 48 hours | Yes |