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A Study to Compare QUTENZA With Pregabalin for the Treatment of Peripheral Neuropathic Pain (PNP) After 8 Weeks of Treatment (ELEVATE)

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ClinicalTrials.gov Identifier: NCT01713426
Recruitment Status : Completed
First Posted : October 24, 2012
Last Update Posted : April 23, 2018
Sponsor:
Information provided by (Responsible Party):
Astellas Pharma Inc ( Astellas Pharma Europe Ltd. )

October 22, 2012
October 24, 2012
April 23, 2018
July 11, 2012
September 26, 2013   (Final data collection date for primary outcome measure)
Proportion of subjects in each arm who achieve at least 30% decrease in the "average pain for the past 24 hours" Numeric Pain Rating Scale (NPRS) score from baseline to week 8 [ Time Frame: Baseline and week 8 ]
Proportion of subjects in each arm who achieve at least 30% decrease in the "average pain for the past 24 hours" Numeric Pain Rating Scale (NPRS) score from baseline to week 8, without change to background chronic pain medication [ Time Frame: Baseline and week 8 ]
Complete list of historical versions of study NCT01713426 on ClinicalTrials.gov Archive Site
  • Proportion of subjects in each arm who achieve "optimal Therapeutic effect" [ Time Frame: Baseline and week 8 ]
    Optimal therapeutic effect is defined as:
    • No change in background chronic pain medication and no discontinuation of study drug due to lack of efficacy or tolerability prior to Week 8
    • At least a 30% reduction in the "average pain for the past 24 hours" NPRS score, from baseline to Week 8, and
    • No moderate or severe adverse drug reactions (ADRs) during the stable Treatment Period
  • Proportion of subjects who achieve at least a 30% decrease in the "average pain for the past 24 hours" [ Time Frame: Baseline to Week 8 ]
    NPRS score from baseline to the mean of all scores recorded between Week 1 (Day 8) and Week 8 (Day 57)
  • Proportion of subjects who achieve at least a 50% decrease in the "average pain for the past 24 hours" [ Time Frame: Baseline to Week 8 ]
    NPRS score from baseline to week 8, and from baseline to the mean of all scores recorded between Week 1 (Day 8) and Week 8 (Day 57)
  • Absolute and percent change in "average pain for the past 24 hours" [ Time Frame: Baseline to Week 8 ]
    NPRS score from baseline to Week 8, and from baseline to the mean of all scores recorded between Weeks 1 to 8
  • Time to onset of pain relief (in days) [ Time Frame: Up to 8 weeks ]
    Assessed by at least a 30% reduction in "average pain for the past 24 hours" NPRS score
  • Overall subject status using Patient Global Impression of Change (PGIC) questionnaire [ Time Frame: At Weeks 4 and 8 ]
  • Change in the Medical Outcomes Study (MOS) 6-Item Cognitive Functioning Scale [ Time Frame: Baseline to Week 8 ]
  • MOS - Sleep Scale [ Time Frame: Baseline to Weeks 4 and 8 ]
  • Change in the EQ-5D-5L (Euroqol-5 dimensions-5 levels) total score [ Time Frame: Baseline to Week 8 ]
  • Treatment satisfaction [ Time Frame: Baseline to Weeks 4 and 8 ]
    As assessed by:
    • Proportion of subjects who discontinue study drug or withdraw from the study due to either a lack of efficacy or tolerability
    • Treatment Satisfaction Questionnaire for Medication (TSQM) questionnaire at Week 4 and Week 8
  • Treatment satisfaction - continuance of treatment [ Time Frame: Week 8 ]
    As assessed by willingness to continue treatment at Week 8
  • Time to reach optimal maintenance dose for pregabalin [ Time Frame: Baseline to Week 8 ]
  • Healthcare Resource use [ Time Frame: Baseline to Week 8 ]
    Number of contacts with health professionals
  • Tolerability (Assessed by the number, severity and duration of ADRs) [ Time Frame: Baseline to Week 8 ]
    Collected as self-rated health-related complaints by the subject and then medically confirmed and causality assigned by the investigator
  • Change in intensity and area of allodynia [ Time Frame: Baseline to Week 8 ]
  • Changes in sensory symptoms [ Time Frame: Baseline to Week 8 ]
    Assessed using Neuropathic Pain Symptom Inventory (NPSI) scores
  • Reduction in pain [ Time Frame: Baseline to Week 8 ]
    By the pattern of sensory symptoms as defined using NPSI scores at baseline.
Same as current
Not Provided
Not Provided
 
A Study to Compare QUTENZA With Pregabalin for the Treatment of Peripheral Neuropathic Pain (PNP) After 8 Weeks of Treatment
Qutenza Versus Pregabalin in Subjects With Peripheral Neuropathic Pain: an Open-label, Randomized, Multicenter, Non-inferiority Efficacy and Tolerability Study

This study is comparing the efficacy and tolerability of Qutenza with that of pregabalin in patients suffering from peripheral neuropathic pain. Treatment allocation will be to one of these treatments and the duration of the study will be about 10 weeks (assuming that from screening to treatment allocation takes 2 weeks). Participants will be asked to complete questionnaires about various aspects relating to their condition throughout the study.

This study will include subjects suffering from Postherpetic Neuralgia, Peripheral Nerve Injury or Non Diabetic peripheral polyneuropathy.

Not Provided
Interventional
Phase 4
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
  • Non-diabetic Painful Peripheral Polyneuropathy
  • Postherpetic Neuralgia (PHN)
  • Peripheral Nerve Injury (PNI)
  • Drug: Qutenza
    Cutaneous patch
    Other Name: Capsaicin
  • Drug: Pregabalin
    Oral capsule
  • Experimental: Qutenza
    Cutaneous patch
    Intervention: Drug: Qutenza
  • Active Comparator: Pregabalin
    Oral capsule
    Intervention: Drug: Pregabalin
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
568
526
September 26, 2013
September 26, 2013   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • 1. Documented diagnosis of probable or definite PNP
  • 2. Localized and well-defined area of PNP, suitable for treatment with QUTENZA
  • 3. Documented diagnosis at the Baseline Visit of either:

    • Postherpetic neuralgia (PHN) with pain persisting at least 6 months since shingles vesicle crusting
    • Peripheral nerve injury (PNI) including post-surgical or post-traumatic neuropathic pain, persisting for a minimum of 3 months
    • Non-diabetic painful peripheral polyneuropathy with pain which has persisted for a minimum of 3 months, including (i) small-fiber neuropathy, as confirmed by quantitative sensory testing (QST), laser evoked potentials (LEP) or skin biopsy, (ii) chemotherapy induced neuropathy in subjects with stable neoplastic disease, (iii) other, adequately characterized painful peripheral polyneuropathy, based on clinical history and examination
  • 4. Average pain score ≥4 during Screening Period, over a minimum of at least 4 consecutive days (using the "average pain for the past 24 hours" Numeric Pain Rating Scale (NPRS) score
  • 5. Intact, non-irritated, dry skin over the painful area(s) to be treated
  • 6. Is either:

    • Naïve to treatment with pregabalin and gabapentin, OR
    • In the opinion of the investigator, has not received an adequate trial of treatment with pregabalin or gabapentin
  • 7. Subject is willing to receive pregabalin or QUTENZA as part of the trial
  • 8. Females of child bearing potential must be willing to use highly effective methods of birth control during the study and for 30 days following study termination

Exclusion Criteria:

  • 1. Significant ongoing or recurrent pain of etiology other than PHN, PNI or non-diabetic painful peripheral polyneuropathy, for example: compression-related neuropathies (e.g. spinal stenosis), radiculopathy, tumor-related pain, fibromyalgia or arthritis
  • 2. Complex Regional Pain Syndrome (CRPS, Type I or II)
  • 3. Neuropathic pain related to previously administered radiotherapy, diabetes mellitus or HIV-AN
  • 4. Neuropathic pain areas located only on the face, above the hairline of the scalp, and/or in proximity to mucous membranes
  • 5. Severe loss of heat sensation in the painful area, indicative of C-fiber denervation
  • 6. Reported daily pain score of 10 on the NPRS for at least 4 days during the Screening Period
  • 7. Past or current history of diabetes mellitus
  • 8. Unstable or poorly controlled hypertension or a recent history of a cardiovascular event which, in the opinion of the investigator, would put the subject at risk of adverse cardiovascular reactions related to the patch application procedure
  • 9. Creatinine clearance (CLcr) < 60mL/min according to the Cockcroft-Gault formula
  • 10. Untreated ongoing generalized anxiety disorder according to DSM-IV or ICD-10 criteria
  • 11. Severe ongoing depression according to DSM-IV or ICD-10 criteria
  • 12. Evidence of cognitive impairment including dementia that may interfere with subject's ability to complete study evaluations and recall pain levels in the past 24 hours
  • 13. Planned elective surgery during the trial
  • 14. Changes to stable neuropathic pain background medication in the 4 weeks prior to the Baseline Visit
  • 15. Any prior receipt of QUTENZA patches, including blinded patches administered as part of a clinical trial
  • 16. Hypersensitivity to capsaicin (i.e., chilli peppers or Over-the-counter [OTC] capsaicin products), any QUTENZA excipients, local anesthetics, or adhesives
  • 17. Treatment with pregabalin or gabapentin within 2 months prior to the Baseline Visit
  • 18. Hypersensitivity to pregabalin or any of the excipients
  • 19. Use of opioids exceeding a total daily dose of morphine of 200 mg/day, or equivalent; or any intravenous opioids or tapentadol, regardless of dose, within 7 days preceding the Baseline Visit
  • 20. Use of any topical pain medication, such as non-steroidal anti-inflammatory drugs, menthol, methyl salicylate, local anesthetics (including patch containing lidocaine), steroids or capsaicin products on the painful areas to be treated within 7 days preceding the Baseline Visit
  • 21. Chemotherapy within 3 months of the Baseline Visit, except maintenance hormone treatment
  • 22. Use of any investigational agent within 30 days prior to Baseline Visit
  • 23. Active substance abuse or history of chronic substance abuse within 1 year prior to screening; or any prior chronic substance abuse (including alcoholism) likely to re-occur during the study period as judged by the investigator
  • 24. Female subjects of child-bearing potential with a positive serum or urine pregnancy test prior to treatment
Sexes Eligible for Study: All
18 Years to 80 Years   (Adult, Older Adult)
No
Contact information is only displayed when the study is recruiting subjects
Armenia,   Austria,   Belarus,   Belgium,   Bulgaria,   Czechia,   Finland,   France,   Germany,   Greece,   Hungary,   Italy,   Poland,   Portugal,   Romania,   Russian Federation,   Slovakia,   Slovenia,   Spain,   Sweden,   Turkey,   United Kingdom
Czech Republic,   Georgia
 
NCT01713426
QTZ-EC-0004
2011-005872-41 ( EudraCT Number )
No
Not Provided
Plan to Share IPD: Undecided
Astellas Pharma Inc ( Astellas Pharma Europe Ltd. )
Astellas Pharma Europe Ltd.
Not Provided
Study Chair: Clinical Study Manager Astellas Pharma Europe Ltd.
Astellas Pharma Inc
April 2018

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP