Study of Efficacy of Lamotrigine in Therapy of Bronchial Asthma

This study has been completed.
Sponsor:
Collaborator:
Rea Rehabilitation Centre, Georgia
Information provided by:
Centre of Chinese Medicine, Georgia
ClinicalTrials.gov Identifier:
NCT00153244
First received: September 8, 2005
Last updated: February 18, 2009
Last verified: February 2009
  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 4

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment
Official Title: Randomised, Placebo Controlled, Double Blind, Parallel Group 3-Months Study of Lamotrigine Efficacy in Asthma Therapy

Resource links provided by NLM:


Further study details as provided by Centre of Chinese Medicine, Georgia:

Primary Outcome Measures:
  • At 3 months of treatment: Change from baseline of the FEV1 and PEFR (also %predicted); Number of patients without asthma symptoms

Secondary Outcome Measures:
  • At 3 months of treatment: FEV1 before and after salbutamol inhalation; Difference in PEF pm-am (in %); The daily (daytime and night-time) symptoms scores; % of symptom free days during the treatment period; Use of other antiasthmatic medication

Estimated Enrollment: 76
Study Start Date: August 2002
Estimated Study Completion Date: May 2003
Detailed Description:

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
Criteria

Inclusion Criteria:

  • Patients must have given their informed consent before commencing the procedures specified in the protocol, indicating that they understand the objectives of the study and are willing to adhere to the procedures described in the protocol.
  • Males or females.
  • Patient aged between 16 and 65 years.
  • Out patients.
  • Non smokers or ex-smokers, having stopped smoking > 1 year.
  • Patients with an established (i.e. at least one year) clinical history of asthma.
  • Absence of long-term remissions of asthma (lasting more than 1 month)
  • Poorly controlled asthma, due to various reasons.
  • Patients with a FEV1 reversibility of at least 12% from initial level after 400 mcg salbutamol inhalation (4 puffs of salbutamol MDI, 100 mcg per puff). Patients whose FEV1 reversibility was 12% within the past 12 months are acceptable, providing that the records are available to the investigator.
  • Patients able to swallow capsules, able to understand and complete diary cards and to record their PEFR using a peak-flow meter.

Exclusion Criteria:

  • Long-term history of smoking (3 years and more)
  • History or presence of cardiovascular, renal, neurologic, psychiatric, liver, immunologic, endocrine, infection or other diseases or dysfunctions if they are clinically significant. A clinically significant disease is defined as one which in the opinion of the investigator may either put the patient at risk because of participation in the study or a disease which may influence the results of the study or the patient's ability to participate in the study.
  • Patients with a recent history (< 1 year) of myocardial infarction and/or (< 3 years) of heart failure or patients with any cardiac arrhythmia requiring drug therapy.
  • History of cancer within the past 5 years.
  • Patients with active tuberculosis with indication for treatment.
  • Patients with a history of cystic fibrosis, bronchiectasis, chronic bronchitis or emphysema.
  • Patients with clinically significant abnormal baseline haematology, blood chemistry or urinalysis or if the abnormal defines a disease listed as an exclusion criterion.
  • Patients with known allergy, side effects, intolerance/hypersensitivity to investigational drug
  • Patients currently using MAO inhibitors, tricyclic antidepressants, antiepileptic drugs, narcotic agents.
  • Pregnant or nursing women and sexually active women with childbearing potential not using a medically approved method of contraception.
  • Patients unlikely, unable or unwilling to comply with the requirements of the protocol.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00153244

Sponsors and Collaborators
Centre of Chinese Medicine, Georgia
Rea Rehabilitation Centre, Georgia
Investigators
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

Additional Information:
No publications provided

ClinicalTrials.gov Identifier: NCT00153244     History of Changes
Other Study ID Numbers: LP-0902-LT-0503
Study First Received: September 8, 2005
Last Updated: February 18, 2009
Health Authority: Georgia: Ministry of Health

Keywords provided by Centre of Chinese Medicine, Georgia:
Bronchial asthma
Lamotrigine
Antiepileptic drug
Efficacy

Additional relevant MeSH terms:
Asthma
Bronchial Diseases
Respiratory Tract Diseases
Lung Diseases, Obstructive
Lung Diseases
Respiratory Hypersensitivity
Hypersensitivity, Immediate
Hypersensitivity
Immune System Diseases
Lamotrigine
Calcium Channel Blockers
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Cardiovascular Agents
Therapeutic Uses
Anticonvulsants
Central Nervous System Agents

ClinicalTrials.gov processed this record on July 24, 2014