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Efficacy and Safety of Oxymorphone Immediate Release in Post-surgical Acute Pain

Phase 3
Completed
Conditions
Acute Pain
Registration Number
NCT00226395
Lead Sponsor
Endo Pharmaceuticals
Brief Summary

The purpose of this study is to evaluate the analgesic efficacy and safety of two doses of oxymorphone immediate release (IR) compared to placebo and oxycodone in post-surgical pain.

Detailed Description

Following abdominal surgery and after sufficient washout from post-surgical analgesia, patients were randomized to one of the following four treatment groups; 1) oxymorphone IR 10 mg, 2) oxymorphone IR 20 mg, 3) oxycodone IR 15 mg, or 4) placebo. Total duration of treatment was 48 hours. Patients were required to take the study medication every 4-6 hours. After the first dose, periodic pain assessments were performed for the first six hours. Subsequently, patients were required to assess their current pain intensity and average pain intensity since the last dose of study medication just prior to every dose.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
320
Inclusion Criteria
  • Male or female patients 18 years of age or older
  • Patients undergoing surgery through an abdominal incision of at least 3 cm who are expected to be hospitalized for at least 36 hours and are expected to subsequently require at least 48 hours of oral opioid therapy.
  • Washout of at least 45 minutes for parenteral and 4 hours for IM analgesia.
  • Initial pain intensity score of at least 50 mm on a 100-mm VAS and a categorical pain rating of moderate or severe on a scale of none, mild, moderate, or severe.
  • Written informed consent.
Exclusion Criteria
  • Known allergy or significant reaction to opioids.
  • History of chronic opioid use or opioid abuse within 6 months prior to study entry.
  • History of alcohol or substance abuse within the last 3 years.
  • Have been a participant in a study of an investigational drug or device within 30 days prior to study entry.
  • Have been a previous participant in an oxymorphone clinical trial.
  • Are currently taking or have taken a monoamine oxidase inhibitor (MAOI) drug within 2 weeks prior to study entry.
  • Are currently taking or have taken St. John's Wort >1000 mg/day within 2 days prior to study entry.
  • Use of long-acting oral and parenteral analgesics (opioid, non-opioid or non-steroidal anti-inflammatory drug [NSAID]) within 12 hours (at least 24 hours for cyclooxygenase-2 [COX 2] analgesics) prior to receiving study medication.
  • Are not stabilized on the following medications for at least 4 weeks prior to dosing: tricyclic antidepressant drugs; serotonin reuptake inhibitors; amphetamines used for attention-deficit hyperactivity disorder (ADHD)
  • Have a history of seizure.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Time to discontinuation due to all causes
Secondary Outcome Measures
NameTimeMethod
- Hourly Pain Intensity Difference Scores
The following are the secondary endpoints during the initial 6 hours following the first dose of study medication:
- 6-Hour Sum of Pain Intensity Differences (SPID; VAS and categorical)
- 6-Hour Total Pain Relief Scores (TOTPAR; VAS and categorical)
- Time (in hours) to First Perceptible Pain Relief
- Time (in hours) to Meaningful Pain Relief
- Hourly Pain Relief Scores
The following are the secondary endpoints during the multiple dosing phase:
- Mean average pain intensity scores collected during the dosing intervals.
- Patient's global evaluation of study medication at the end of study.
- Physician's global evaluation of study medication at the end of study.
- Mean current pain intensity (VAS) collected during the dosing intervals.

Trial Locations

Locations (21)

Univ. Pittsburgh Hospital

🇺🇸

Pittsburgh, Pennsylvania, United States

Univ. Pittsburgh Medical center

🇺🇸

Pittsburgh, Pennsylvania, United States

Huntington Memorial Hospital

🇺🇸

Pasadena, California, United States

Brookwood Medical Center

🇺🇸

Birmingham, Alabama, United States

The Medical Center, Dept. Clinical research

🇺🇸

Birmingham, Alabama, United States

Arrowhead Community Hospital

🇺🇸

Phoenix, Arizona, United States

John C Lincoln Hospital

🇺🇸

Phoenix, Arizona, United States

Palm West Hospital

🇺🇸

Palm Springs, Florida, United States

Sacred Heart Hospital

🇺🇸

Pensacola, Florida, United States

The Methodist Hospital

🇺🇸

Houston, Texas, United States

Cottonwood Hospital

🇺🇸

Salt Lake City, Utah, United States

LDS Hospital

🇺🇸

Salt Lake City, Utah, United States

McKay-Dee Hospital

🇺🇸

Salt Lake City, Utah, United States

Montgomery Women's Health Associates

🇺🇸

Montgomery, Alabama, United States

Paradise Valley Hospital

🇺🇸

Phoenix, Arizona, United States

Glendale Adventist Medical Center

🇺🇸

Glendale, California, United States

Duke University Medical Center

🇺🇸

Durham, North Carolina, United States

Saddleback Memorial Medical Center

🇺🇸

Laguna Hills, California, United States

Forsyth Medical Center

🇺🇸

Winston-Salem, North Carolina, United States

Medical Park Hospital

🇺🇸

Winston-Salem, North Carolina, United States

Memorial Hermann Memorial City Hospital

🇺🇸

Houston, Texas, United States

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