Safety, Effectiveness, and Impact on Quality of Life on Long-Term Administration of OROS Hydromorphone Slow-Release in Patients With Chronic Low Back Pain

Condition(s) targeted: Low Back Pain

Intervention: OROS hydromorphone HCI SR (slow release) (Drug)

Phase: Phase 3

Status: Completed

Sponsored by: Alza Corporation, DE, USA

Official(s) and/or principal investigator(s):
Alza Corporation Clinical Trial, Study Director, Affiliation: Alza Corporation, DE, USA

The purpose of this open-label, extension study is to characterize the safety, effectiveness, and impact on quality of life measures of long-term repeated dosing of OROS hydromorphone slow release (8, 16, 32 and 64 mg tablets) in patients with chronic low back pain.

Official title: Safety, Efficacy and Impact on Quality of Life of Long-Term Administration of Dilaudid CR (Hydromorphone HCI) in Patients With Chronic Low Back Pain

Study design: Treatment, Randomized, Open Label, Single Group Assignment, Safety/Efficacy Study

Primary outcome: The daily pain relief rating obtained during the study.(six months)

Secondary outcome: Differences from first visit to each subsequent visit in Brief Pain Inventory (BPI) ratings, sleep scores and quality of life questionnaires.

Detailed description: This open label, extension study characterized the safety, effectiveness, and impact on quality of life of OROS hydromorphone slow release with long-term repeated dosing among patients with chronic low back pain, who previously completed short-term Study DO-127 with OROS hydromorphone slow release. Up to 150 patients were to be enrolled and evaluated. Patients were enrolled in this study immediately following Study DO-127. Patients continued their therapy with OROS hydromorphone slow release at the stable dose previously identified in the short-term study. The patient's initial prescribed dose of OROS hydromorphone slow release in Study DO-127X was the same as the last dose of OROS hydromorphone slow release in Study DO-127. Patients returned monthly for evaluations during this extension interval. Adjustments to dose were performed as needed, at the Investigator's discretion. The duration of this study was six months. Safety assessments included vital signs and physical examination at start, during and end of study.

8, 16, 32 and 64 mg tablets of OROS hydromorphone (dose will be at Investigators' discretion) slow release tablets were taken orally daily for the duration of the six month study

Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Patients who have chronic low back pain who have successfully completed short-term

Study DO-127 with OROS hydromorphone slow release

- Patients who require at least 8 mg of hydromorphone HCI (slow release) every 24 hours

for the management of chronic low back pain

- Patients whose opioid requirements have been stable as demonstrated in short-term

Study DO-127 with OROS hydromorphone slow release

Exclusion Criteria:

- Patients intolerant of or hypersensitive to hydromorphone (or other opioid agonists)

- Patients who are pregnant or breast-feeding

- Patients with any gastrointestinal disorder, including pre-existing severe GI

narrowing (pathologic or iatrogenic) that may affect the absorption or transit of orally administered drugs

- Patients with significant CNS disorder, including but not limited to head injury,

intracranial lesion, increased intracranial pressure, seizure disorder, stroke within the past 6 months, disorders of cognition, any clinically significant impaired renal or hepatic function, Addison's disease, hypothyroidism, prostatic hypertrophy, or urethral stricture

- Patients who may be at risk for serious decreases in blood pressure upon taking an

opioid analgesic

Ending date: June 2001
Last updated: March 17, 2008