Safety and Efficacy Study of Hydromorphone Hydrochloride by Intrathecal Administration
CompletedPhase 3NCT01709721
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The purpose of this study is to determine the safety and efficacy of hydromorphone hydrochloride by intrathecal administration using a programmable implantable pump.
Study details
- Official title
- A Controlled, Two-Arm, Parallel Group, Randomized Withdrawal Study to Assess the Safety and Efficacy of Hydromorphone Hydrochloride Delivered by Intrathecal Administration Using a Programmable Implantable Pump
- Conditions
- Management of Chronic Pain
- Interventions
- Drug: Hydromorphone Hydrochloride
- Device: Programmable Implantable pump
- Sponsor
- Piramal Critical Care, Ltd.
- Start date
- 2013-02
- Primary completion
- 2018-02
- Sex
- All
- Age range
- from 18 Years to 75 Years
- Results posted
- Yes, on ClinicalTrials.gov
- Countries
- United States
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: Subjects must meet all of the following criteria to be included: 1. Subject must be at least 18 years of age and no more than 75 years old. 2. Clinically diagnosed with chronic pain for at least a 6-month period. 3. Subject is presently on intrathecal pain medication and has a SynchroMed II Implantable pump or meets clinical criteria for implantation of a SynchroMed II Implantable pump. Subjects who are naïve to intrathecal therapy, may be enrolled 2-weeks after pump implantation. 4. Subject agrees to sign a Pain Treatment Agreement (Narcotic Contract) limiting narcotic prescriptions to the study physician. 5. Subject must be cognitively intact and, in the opinion of the investigator, capable of participation in the trial. 6. Female subjects of child-bearing potential must agree to use a medically acceptable and effective double-barrier method of birth control. 7. Subjects with existing SynchroMed II Implantable pumps and are reasonably expected to benefit from intrathecal opioid therapy only. 8. Subjects who are capable of receiving an MRI with or without contrast or CT myelogram, if required by the study protocol. 9. Provides written Ethics Committee approved informed consent. 10. Willing to comply with all study procedures and requirements.. Exclusion Criteria: Subjects meeting any of the following criteria will be excluded: 1. Women who are pregnant or are breast-feeding 2. Subjects who have participated in an investigational drug or device trial within 4 weeks prior to enrollment. 3. Subject has any known or suspected allergy to hydromorphone or to the materials of the infusion pump or intrathecal catheter. 4. Subject is scheduled for a pump or catheter replacement within 6 months of their enrollment into the trial. 5. Subject has a history of dependence and abuse of opioids, stimulants, alcohol, or benzodiazepines, as defined by DSM-IV criteria, within the past year (physical dependence on prescribed opioid analgesics is allowed but abuse of opioids according to DSM-IV is not permitted, i.e. opioid addiction for recreational use). 6. Subjects who show signs of active systemic infection. 7. Subjects with a metastatic cancer to the spinal canal or a known central nervous system contraindication to intrathecal therapy. 8. Subject has a condition requiring diathermy procedures. 9. Subject has a life expectancy of less than 12 months. 10. Subject cannot independently comprehend and participate in the required assessments, including res…
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01709721