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Study of D-Methadone in Patients With Chronic Pain

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Memorial Sloan Kettering Cancer Center
ClinicalTrials.gov Identifier:
NCT00588640
First received: December 22, 2007
Last updated: June 29, 2016
Last verified: June 2016
  Purpose
The purpose of this study is to determine the safest dose of d-methadone that can be given, without causing severe side effects in most patients with chronic pain. Patients are being asked to participate in the Phase I portion of this study.

Condition Intervention Phase
Pain Bladder Cancer Breast Cancer CNS Cancer Colon Cancer Esophageal Cancer Pancreatic Cancer Prostate Cancer Uterine Cancer Head and Neck Cancer Eye Cancer Otorhinolaryngologic Neoplasms Drug: d-Methadone Drug: D-methadone Drug: placebo Phase 1 Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: A Phase I/II Study of D-Methadone in Patients With Chronic Pain

Resource links provided by NLM:


Further study details as provided by Memorial Sloan Kettering Cancer Center:

Primary Outcome Measures:
  • Number Who Reached a Safe Dose [ Time Frame: 2 years ]
    The number of patients who reached a safe and well tolerated dose of d-methadone


Enrollment: 10
Study Start Date: October 2004
Study Completion Date: July 2008
Primary Completion Date: July 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Phase I, Group
This is an open label dose-ranging trial. The first cohort of 8 patients will receive 40mg of d-methadone every 12 hours.
Drug: d-Methadone
8 subjects to receive 40 mg d-Methadone twice a day
Experimental: Phase II, Group I
patients receiving around the clock opioid therapy-No patients were accrued to this group
Drug: D-methadone
After randomization, patients will take the study drug or placebo for 12 days and then they will cross-over to the opposite arm for another 12 days. The study will end on day 24.
Experimental: Phase II, Group II
patients not receiving around the clock opioid therapy.No patients were accrued to this group
Drug: placebo
After randomization, patients will take the study drug or placebo for 12 days and then they will cross-over to the opposite arm for another 12 days. The study will end on day 24.

  Eligibility

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

Phase I and Phase II portions of the study:

  • 18 years of age or older
  • Chronic pain with average 24 hour intensity rated at least 3 on a verbal numerical scale from 0-10 during the 24 hours prior to study entry.
  • Give informed consent to participate in this study.
  • Karnofsky Performance Score (KPS) >= to 80
  • Negative urine pregnancy test, verified by the study nurse, at study entry (for women of child-bearing potential). Patients must also use a medically approved contraceptive method during the study period.

Phase I only:

  • Responsible companion living with patient during study.

Phase II only:

  • Group 1 -- Patients must be taking chronic opioid therapy (long acting morphine, long acting oxycodone, transdermal fentanyl) at a stable dose for a minimum of four days. The dose of as needed short acting opioid does not need to be stable.
  • Group 2 -- Patients must not be receiving opioids and must have cancer related neuropathic pain secondary to post-chemotherapy peripheral neuropathy, post-radiation and/or post surgical plexopathy, radiculopathy or neuropathy, or post- herpetic neuralgia.

Exclusion Criteria:

Phase I and Phase II:

  • Known hypersensitivity to methadone
  • Patient taking methadone or with a history of methadone treatment within one month of study enrollment.
  • Patient that requires changes in the dose of one of the following medications within 2 weeks of study enrollment:

    • Abacavir,
    • Benzodiazepines,
    • Carbamazepine,
    • Efavirenz,
    • Fluconazole,
    • Fluvoxamine,
    • FOS amprenavir,
    • Fosphenytoin,
    • Naltrexone,
    • Nelfinavir,
    • Nevirapine,
    • Phenytoin,
    • Rifampin,
    • Rifapentine,
    • Risperidone,
    • Ritonavir,
    • St. John's Wort,
    • Zidovudine
  • Hepatic function tests (SGOT, alkaline phosphatase, bilirubin) greater than 2 times the upper limit of normal or creatinine greater than 1.4 within 30 days of study entry.
  • Neurologic or psychiatric disease sufficient, in the investigator's opinion, to compromise data collection.
  • Women who are pregnant or nursing.
  • Women of childbearing potential who do not agree to use a medically recognized method of contraception during the study period.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00588640

Locations
United States, New York
Memorial Sloan Kettering Cancer Center
New York, New York, United States, 10065
Sponsors and Collaborators
Memorial Sloan Kettering Cancer Center
Investigators
Principal Investigator: Natalie Moryl, MD Memorial Sloan Kettering Cancer Center
  More Information

Additional Information:
Responsible Party: Memorial Sloan Kettering Cancer Center
ClinicalTrials.gov Identifier: NCT00588640     History of Changes
Other Study ID Numbers: 01-017
Study First Received: December 22, 2007
Results First Received: December 17, 2015
Last Updated: June 29, 2016

Keywords provided by Memorial Sloan Kettering Cancer Center:
Pain
HEENT cancer

Additional relevant MeSH terms:
Pancreatic Neoplasms
Head and Neck Neoplasms
Urinary Bladder Neoplasms
Esophageal Neoplasms
Chronic Pain
Uterine Neoplasms
Eye Neoplasms
Otorhinolaryngologic Neoplasms
Digestive System Neoplasms
Neoplasms by Site
Neoplasms
Endocrine Gland Neoplasms
Digestive System Diseases
Pancreatic Diseases
Endocrine System Diseases
Urologic Neoplasms
Urogenital Neoplasms
Urinary Bladder Diseases
Urologic Diseases
Gastrointestinal Neoplasms
Esophageal Diseases
Gastrointestinal Diseases
Pain
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms
Genital Neoplasms, Female
Uterine Diseases
Genital Diseases, Female
Eye Diseases

ClinicalTrials.gov processed this record on August 18, 2017