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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: | NCT00153244 |
Purpose
The purpose of this study is to determine whether antiepileptic drug lamotrigine is effective in the treatment of chronic asthma.
| Condition | Intervention | Phase |
|---|---|---|
|
Bronchial Asthma |
Drug: Lamotrigine |
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 Lamotrigine Efficacy in Asthma Therapy |
| Estimated Enrollment: | 76 |
| Study Start Date: | August 2002 |
| Estimated Study Completion Date: | May 2003 |
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 double-blind placebo-controlled 3-month trial for evaluation of lamotrigine efficacy in therapy of poorly controlled bronchial asthma. Lamotrigine is antiepileptic drug of new generation, produced by Glaxo SmithCline.
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, PhD | Rea Rehabilitation Centre, Georgia |
| Study Chair: | Manana Tchaia, MD | Centre of Chinese Medicine |
| Study Director: | Tamara Tchelidze, MD | CRO Evidence |
More Information
| Study ID Numbers: | LP-0902-LT-0503 |
| Study First Received: | September 8, 2005 |
| Last Updated: | February 18, 2009 |
| ClinicalTrials.gov Identifier: | NCT00153244 History of Changes |
| Health Authority: | Georgia: Ministry of Health |
|
Bronchial asthma Lamotrigine Antiepileptic drug Efficacy |
|
Bronchial Diseases Immune System Diseases Molecular Mechanisms of Pharmacological Action Asthma Calcium Channel Blockers Cardiovascular Agents Pharmacologic Actions Membrane Transport Modulators Lung Diseases, Obstructive |
Hypersensitivity Respiratory Tract Diseases Therapeutic Uses Lung Diseases Hypersensitivity, Immediate Lamotrigine Central Nervous System Agents Anticonvulsants Respiratory Hypersensitivity |