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| Sponsor: | Centre of Chinese Medicine, Georgia |
|---|---|
| Collaborator: |
Rea Rehabilitation Centre, Georgia |
| Information provided by: | Centre of Chinese Medicine, Georgia |
| ClinicalTrials.gov Identifier: | NCT00153283 |
Purpose
The purpose of this study is to determine whether antiepileptic drug gabapentin is effective in the treatment of chronic asthma.
| Condition | Intervention | Phase |
|---|---|---|
|
Bronchial Asthma |
Drug: Gabapentin |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Efficacy Study |
| Official Title: | Randomised, Placebo Controlled, Double Blind, Parallel Group 3-Months Study of Gabapentin Efficacy in Asthma Therapy |
| Estimated Enrollment: | 68 |
| Study Start Date: | September 2003 |
| Estimated Study Completion Date: | April 2004 |
Effective therapy of asthma still remains quite serious problem. According GINA definition, asthma is an inflammatory disorder. Consequently, modern pharmacotherapy of asthma provides wide use of anti-inflammatory drugs. But asthma also is a paroxysmal disorder: many specialists and even some guidelines underline paroxysmal clinical picture of asthma. Besides this, according to some authors, neurogenic inflammation may play important role in asthma mechanism. But some other neurogenic inflammatory paroxysmal disorders exist, and they are migraine and trigeminal neuralgia. Some antiepileptic drugs, like carbamazepine and valproate, are very effective in therapy of migraine and trigeminal neuralgia - more than in 80% of cases. If bronchial asthma also is paroxysmal inflammatory disease, like migraine and trigeminal neuralgia, it is possible that some antiepileptic drugs also are very effective in asthma therapy.
We performed a double-blind, placebo-controlled 3-month trial for evaluation of gabapentin efficacy in therapy of bronchial asthma. Gabapentin is antiepileptic drug of new generation, produced by Pfizer.
Comparison: Patients received investigational drug in addition to their usual routine antiasthmatic treatment, compared to patients received placebo in addition to their usual routine antiasthmatic treatment.
Eligibility| Ages Eligible for Study: | 16 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Principal Investigator: | Merab Lomia, MD | "Rea" Rehabilitation Centre |
| Study Director: | Tamara Tchelidze, MD | CRO Evidence |
| Study Chair: | Manana Tchaia, MD | Centre of Chinese Medicine |
More Information
| Study ID Numbers: | LTP-0904-GP-0404 |
| Study First Received: | September 8, 2005 |
| Last Updated: | February 18, 2009 |
| ClinicalTrials.gov Identifier: | NCT00153283 History of Changes |
| Health Authority: | Georgia: Ministry of Health |
|
Bronchial asthma Gabapentin Antiepileptic drug Efficacy |
|
Neurotransmitter Agents Bronchial Diseases Molecular Mechanisms of Pharmacological Action Gabapentin Anti-Dyskinesia Agents Physiological Effects of Drugs Psychotropic Drugs Antiparkinson Agents Calcium Channel Blockers Excitatory Amino Acid Agents Membrane Transport Modulators Hypersensitivity Lung Diseases, Obstructive Respiratory Tract Diseases Sensory System Agents |
Therapeutic Uses Analgesics Excitatory Amino Acid Antagonists Tranquilizing Agents Immune System Diseases Central Nervous System Depressants Asthma Cardiovascular Agents Antimanic Agents Pharmacologic Actions Lung Diseases Hypersensitivity, Immediate Anti-Anxiety Agents Peripheral Nervous System Agents Central Nervous System Agents |