Ketamine Hydrochloride and Best Pain Management in Treating Cancer Patients With Neuropathic Pain
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|ClinicalTrials.gov Identifier: NCT01316744|
Recruitment Status : Unknown
Verified March 2011 by National Cancer Institute (NCI).
Recruitment status was: Recruiting
First Posted : March 16, 2011
Last Update Posted : May 13, 2011
RATIONALE: Ketamine hydrochloride may lessen neuropathic pain in patients with cancer. It is not yet known whether ketamine hydrochloride given together with the best pain management is more effective than a placebo given together with the best pain management in treating neuropathic pain in patients with cancer.
PURPOSE: This randomized phase III trial is studying ketamine hydrochloride given together with the best pain management to see how well it works compared with giving a placebo together with the best pain management in treating cancer patients with neuropathic pain.
|Condition or disease||Intervention/treatment||Phase|
|Cancer||Drug: ketamine hydrochloride Other: pharmacogenomic studies Other: questionnaire administration Procedure: assessment of therapy complications Procedure: quality-of-life assessment||Phase 3|
- To determine whether ketamine hydrochloride given in addition to best standard pain management improves malignant neuropathic pain compared to best standard pain management alone in patients with cancer.
- To compare initial treatment benefit (at day 4 of assessment period of 16 days) using the sensory component of the McGill Short-Form Questionnaire.
- To compare difference in overall pain between the study arms based on the pain-intensity visual-analogue score (VAS).
- To compare difference in neuropathic pain between the study arms based on the Leeds Assessment of Neuropathic Symptoms and Signs (LANSS) pain scale.
- To assess worst pain score (index neuropathic site) between the two arms.
- To compare patient distress between the two arms based on NCCN Distress Thermometer.
- To assess the side effects and tolerability of trial drug.
- To assess the effect of intervention on quality of life scores (based on Euroqol thermometer), anxiety and depression (based on HADS), and opioid requirements.
OUTLINE: This is a multicenter study.
- Stage 1 (Run-in Period): Opioid doses are optimized, under a defined schedule, for up to a maximum of 10 days to ensure that all patients are on an optimized and stable regimen* prior to randomization. Following the run-in-period, patients undergo reassessment. Patients who have improved pain scores (i.e., < 4/10 on the visual-analogue score in the past 24 hours or < 5 McGill Sensory Scale Score) are taken off the study. Patients whose scores have not improved continue on to Stage 2 of the study.
NOTE: *Stable regimen is defined as the same dose of controlled release and no more variation than 2 breakthrough opioid doses over the normal for that patient for a period of 48 hours.
Stage 2 (Titration Period): Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients receive oral ketamine hydrochloride 4 times a day. Doses are titrated until when analgesia is achieved or individual side effects appear, for up to 14 days.
- Arm II: Patients receive an oral placebo 4 times a day. Doses are titrated until when analgesia is achieved or individual side effects appear, for up to 14 days.
- Stage 3 (Assessment Period): Patients receive the trial medication (i.e., ketamine hydrochloride or placebo) at the fixed optimum dose (reached during the titration period) for 16 days.
Patients are allowed to receive breakthrough opioids at any time during the study.
Patients complete quality-of-life and pain-assessment questionnaires periodically. Some patients may undergo blood sample collection periodically for pharmacogenomics studies at a later date.
Peer Reviewed and Funded or Endorsed by Cancer Research UK.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||214 participants|
|Primary Purpose:||Supportive Care|
|Official Title:||A Randomized Double-Blind Controlled Trial of Ketamine Versus Placebo in Conjunction With Best Pain Management in Neuropathic Pain in Cancer Patients|
|Study Start Date :||April 2009|
|Estimated Primary Completion Date :||October 2011|
- Time to treatment failure
- Initial treatment benefit (at day 4 of assessment period of 16 days) using the sensory component of the McGill Short-Form Questionnaire
- Difference in overall pain between the study arms based on the visual-analogue score
- Difference in neuropathic pain between the study arms based on the Leeds Assessment of Neuropathic Symptoms and Signs (LANSS) pain scale
- Worst pain score (index neuropathic site) in the previous 24 hours (between the two arms) at study baseline and then during study assessment period
- Patient distress between the two arms based on NCCN Distress Thermometer
- Side effects and tolerability of trial drug
- Effect of the intervention on quality-of-life scores (based on Euroqol thermometer), anxiety and depression (based on HAD scale), and opioid requirements
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01316744
|Royal Brompton Hospital||Recruiting|
|London, England, United Kingdom, SW3 6NP|
|Contact: Contact Person 44-207-886-6011 email@example.com|
|Edinburgh Cancer Centre at Western General Hospital||Recruiting|
|Edinburgh, Scotland, United Kingdom, EH4 2XR|
|Contact: Contact Person 44-131-777-3520 firstname.lastname@example.org|
|Beatson West of Scotland Cancer Centre||Recruiting|
|Glasgow, Scotland, United Kingdom, G12 0YN|
|Contact: Contact Person 44-141-301-7033 email@example.com|
|Principal Investigator:||Marie T. Fallon||Edinburgh Cancer Centre at Western General Hospital|
|Principal Investigator:||Barry J.A. Laird, MD||Edinburgh Cancer Centre at Western General Hospital|