Efficacy and Safety of Gabapentin/B-complex Versus Pregabalin in Diabetic Peripheral Neuropathy Pain Management
Overview[ - collapse ][ - ]
Purpose | This is a multicenter, randomized, open-label, parallel, Phase 4 clinical trial to compare efficacy and safety of gabapentin/B-complex versus pregabalin in diabetic peripheral neuropathy pain (DPNP) management. |
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Condition | Diabetic Peripheral Neuropathic Pain |
Intervention | Drug: Gabapentin/B-complex Drug: Pregabalin |
Phase | Phase 4 |
Sponsor | Merck KGaA |
Responsible Party | Merck KGaA |
ClinicalTrials.gov Identifier | NCT01364298 |
First Received | May 31, 2011 |
Last Updated | December 18, 2013 |
Last verified | December 2013 |
Tracking Information[ + expand ][ + ]
First Received Date | May 31, 2011 |
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Last Updated Date | December 18, 2013 |
Start Date | April 2011 |
Estimated Primary Completion Date | July 2012 |
Current Primary Outcome Measures | Change From Baseline in Average Numeric Pain Intensity Scale (NPIS) Score at Day 84 [Time Frame: Baseline and Day 84 (Week 12)] [Designated as safety issue: No]An average NPIS pain score (daily average records of the past seven days) was evaluated. Numeric pain intensity scale (NPIS) is a 11-point scale, with 0 representing no pain and 10 representing the worst possible pain. The participants were asked to mark the number that best represents the current level of pain they have experienced during the previous 24 hours. Change from baseline data has been calculated as value at baseline minus value at Day 84. |
Current Secondary Outcome Measures |
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Descriptive Information[ + expand ][ + ]
Brief Title | Efficacy and Safety of Gabapentin/B-complex Versus Pregabalin in Diabetic Peripheral Neuropathy Pain Management |
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Official Title | Multicenter, Randomized, Open-label, Parallel Group, Phase IV Study to Compare the Efficacy and Safety of Gabapentin/B-complex Versus Pregabalin in the Management of Diabetic Peripheral Neuropathic Pain |
Brief Summary | This is a multicenter, randomized, open-label, parallel, Phase 4 clinical trial to compare efficacy and safety of gabapentin/B-complex versus pregabalin in diabetic peripheral neuropathy pain (DPNP) management. |
Detailed Description | Primary Objective: To compare the efficacy of gabapentin/B-complex versus pregabalin administered for 12 weeks in the treatment of pain in mild to moderate diabetic peripheral neuropathy (DPN) of acute or chronic presentation. Secondary Objectives: To determine the safety and tolerability of gabapentin/B-complex versus pregabalin administered for 12 weeks in the treatment of pain in mild to moderate DPN of acute or chronic presentation. Subjects will be randomized in a 1:1 ratio to receive gabapentin/B-complex or pregabalin. The duration of treatment per subject will be 12 weeks. |
Study Type | Interventional |
Study Phase | Phase 4 |
Study Design | Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment |
Condition | Diabetic Peripheral Neuropathic Pain |
Intervention | Drug: Gabapentin/B-complex Gabapentin/B-complex (Gavindo®) tablet will be administered orally at an initial dose of 300 milligram per day (mg/day) on Day 1, followed by 600 mg/day (one 300 milligram [mg] tablet every 12-hour) on Day 2, then 900 mg/day (one 300 mg tablet every 8-hour) on Day 7, then 1800 mg/day (two 300 mg tablets every 8-hour) on Day 21, then 2700 mg/day (three 300 mg tablets every 8-hour) on Day 35, and finally 3600 mg/day (four 300 mg tablets every 8-hour) on Days 56 and 84. Maximum dose allowed will be 3600 mg/day. The total duration of treatment will be 84 days (12 weeks). Other Names: Gavindo®Drug: Pregabalin Pregabalin (Lyrica®) capsule will be administered orally at an initial dose of 150 mg/day (one 75 mg capsule every 12-hour) from Day 1 to 7, followed by 300 mg/day (one 150 mg capsule every 12-hour) on Day 7, then 600 mg/day (two 150 mg capsule every 12-hour) on Days 21, 35, 56 and 84. Maximum dose allowed will be 600 mg/day. The total duration of treatment will be 84 days (12 weeks). Other Names: Lyrica® |
Study Arm (s) |
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Recruitment Information[ + expand ][ + ]
Recruitment Status | Completed |
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Estimated Enrollment | 353 |
Estimated Completion Date | July 2012 |
Estimated Primary Completion Date | July 2012 |
Eligibility Criteria | Inclusion Criteria: - Females or males undististincally - Age 18 to 70 years - Signed informed consent (IC) by the subject - Diabetes mellitus (DM) Type 1 or 2 - Pain due to sensorial or motor DPN of low to moderate intensity, greater than or equal to (>=) 1 year of evolution and less than or equal to (=<)5 years of being diagnosed - Subjects who score >=40 millimeter (mm) in the visual analogue scale (VAS) of the McGill pain questionnaire (MPQ) at selection and Baseline visit, and who complete on a daily basis the numeric pain intensity (NPI) (at least 4 days a week) during the week previous to randomization and whose daily mean score is of at least 4, during the 7 days previous to randomization (with a wash-out period) - Normal chest radiography - Stable hypoglycemic treatment, at least 6 weeks before randomization - Glycosylated hemoglobin (HbA1c) =<10 percent at selection visit - Women must not be pregnant and must not have pregnancy plans during the period of the study duration - Subjects not medicated or under analgesic stable medication during a minimum of 4 weeks, where no acceptable relief of pain is achieved; in the last case, with the corresponding wash-out period - Women of childbearing age must submit a negative pregnancy test before treatment randomization and should use a contraceptive method medically accepted, during the study period Exclusion Criteria: - Suicide risk defined as a score of 2 or higher, in question 9 of the beck depression test - Congestive heart failure Class III or IV of the New York Heart Association (NYHA) - Subjects with serious or unstable coronary heart disease, hepatic, kidney, respiratory, hematological alterations, problems with peripheral vascular disease, or other medical or psychiatric conditions that can put in risk the participation of the subject in the study or that may lead to hospitalization during the study period - Any condition that may lead to confusion of the diagnostic of painful DPN, in particular amputations -other than fingers/toes-, not diabetic neurological disorder and skin conditions that may affect sensation at the painful limbs - Subjects with Baseline calculated creatinine clearance less than (<) 60 milliliter per minute (mL/min), Baseline leukocyte count < 2,500 per cubic millimeter (/mm^3), Baseline neutrophils count < 1,500/mm^3 or platelets < 100 * 10^3 /mm^3 - Subjects who have participated previously in some other study of pregabalin or gabapentin or gabapentin/B-complex, during 30 days previous to selection - Subjects with encephalopathy caused by ammonia with alterations in the cycle of urea - Subjects with uncontrolled closed-angle glaucoma - Subject with presence of a disorder or an anticonvulsant treatment - Breastfeeding women or during the first 3 months postpartum - Morbid obesity (body mass index [BMI] >=40) - Glycosylated hemoglobin (HbA1c) greater than (>) 10 percent - Major surgery 3 months previous to randomization - Any surgery 2 weeks previous to randomization process, or programmed during the study period should have been authorized by the Sponsor or appointed representative - Blood donors 60 days previous to randomization - Abuse or dependency of alcohol, narcotics, opioids or any other addictive substances, or energizing drinks - History of hypersensitivity to the drugs in the study or drugs with similar chemical structures - History or suspicion of lack of trust, poor cooperation of lack of compliance of medical treatments - Subjects with arthritis, sciatic, fibromyalgia, restless leg syndrome, non-neuropathic muscle-skeletal pain or back chronic pain |
Gender | Both |
Ages | 18 Years |
Accepts Healthy Volunteers | No |
Contacts | Not Provided |
Location Countries | Mexico |
Administrative Information[ + expand ][ + ]
NCT Number | NCT01364298 |
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Other Study ID Numbers | EMR200054-603 CL028 |
Has Data Monitoring Committee | Yes |
Information Provided By | Merck KGaA |
Study Sponsor | Merck KGaA |
Collaborators | Merck S.A. de C.V., Mexico |
Investigators | Study Director: Clinical Research Manager Merck S.A de C.V, Mexiko, an affiliate of Merck KGaA, Darmstadt, Germany |
Verification Date | December 2013 |
Locations[ + expand ][ + ]
Research Site | Mexico City, Mexico |
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