Efficacy of Albuterol in the Treatment of Congenital Myasthenic Syndromes
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Purpose
The study tests the notion that patients suffering from certain types of congenital myasthenic syndromes are benefitted by the use of Albuterol at doses used in clinical practice.
| Condition | Intervention |
|---|---|
|
Congenital Myasthenic Syndrome |
Drug: Albuterol |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
- Name: Efficacy of albuterol in the treatment of congenital myasthenic syndromes [ Time Frame: 3 years ] [ Designated as safety issue: Yes ]The primary outcome measures pertain to evaluating the improvement in the patient's strength
| Estimated Enrollment: | 50 |
| Study Start Date: | September 2010 |
| Estimated Study Completion Date: | September 2013 |
| Estimated Primary Completion Date: | September 2013 (Final data collection date for primary outcome measure) |
-
Drug: Albuterol
The aim of the proposal is to evaluate the effects of albuterol, an adrenergic agonist, in the treatment of congenital myasthenic syndromes (CMS). Over the past 2 decades I found that some CMS patients refractory to or worsened by cholinergic agonists, namely those suffering from defects in acetylcholinesterase (AChE) or Dok-7, respond to ephedrine, a medication used for over half-a-century in the treatment of autoimmune myasthenia gravis. After ephedrine became unavailable, I treated the same type of patients with albuterol in doses ranging from 4 mg daily to twice daily for adults; the dose for children 6 to 12 years is 2 mg two or three times daily; the dose for children 2to 6 years is 0.1 mg/kg/day (maximum 2 mg) three times daily. Evaluation of the effects of the medications are based on the Table shown below.
Name:
Mayo Clinic no:
Date of this report: (dd/mm/yyyy):
Before taking Albuterol ER On Albuterol (date of this report)
- Current daily dose of albuterol:
Dates when started (d/m/year) Daily dose Distance in feet walked without stopping to rest Number of steps climbed without stopping to rest Difficult to sit up from lying on back* Difficult to rise from sitting* Difficult to speak or swallow* Shortness of breath on exertion* Shortness of breath at night* Weakness of arm or hand muscles * Weakness of leg or foot muscles*
*Rate as mild, moderate, severe Describe below any additional changes in your condition such as arm elevation time, number of deep knee bends before having to stop, or in activities of daily living relevant to the effects of the treatment. Also indicate any unwanted side effects of the medication. Continue on other side or separate page if necessary. Return this questionnaire to Dr. Andrew Engel (email:schaefer.cleo@mayo.edu) ,after treatment with albuterol for 1 month and then monthly thereafter, or mail to Dr. Andrew Engel, Department of Neurology, Mayo Clinic, Rochester, MN 55905.
Eligibility| Ages Eligible for Study: | 2 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Diagnosis of congenital myasthenic syndrome substantiated by typical clinical history, seronegativity to AChR and MuSK, and evidence of a decremental EMG response.
Exclusion Criteria:
- Uncontrolled hypertension, arrhythmias, or other significant cardiac disease.
Contacts and Locations| United States, Minnesota | |
| Mayo Clinic | Recruiting |
| Rochester, Minnesota, United States, 55905 | |
| Contact: Andrew G. Engel, MD 507-284-5102 age@mayo.edu | |
| Principal Investigator: Andrew G. Engel, MD | |
More Information
No publications provided
| Responsible Party: | Andrew G. Engel, MD, Mayo Clinic Rochester |
| ClinicalTrials.gov Identifier: | NCT01203592 History of Changes |
| Other Study ID Numbers: | 10-004529 |
| Study First Received: | September 15, 2010 |
| Last Updated: | February 25, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Mayo Clinic:
|
Congenital myasthenic syndrome Albuterol Neuromuscular transmission |
Additional relevant MeSH terms:
|
Lambert-Eaton Myasthenic Syndrome Myasthenic Syndromes, Congenital Paraneoplastic Syndromes, Nervous System Paraneoplastic Syndromes Nervous System Neoplasms Neoplasms by Site Neoplasms Autoimmune Diseases of the Nervous System Nervous System Diseases Neurodegenerative Diseases Neuromuscular Junction Diseases Neuromuscular Diseases Autoimmune Diseases Immune System Diseases Genetic Diseases, Inborn |
Albuterol Tocolytic Agents Reproductive Control Agents Physiological Effects of Drugs Pharmacologic Actions Therapeutic Uses Adrenergic beta-2 Receptor Agonists Adrenergic beta-Agonists Adrenergic Agonists Adrenergic Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Bronchodilator Agents Autonomic Agents Peripheral Nervous System Agents |
ClinicalTrials.gov processed this record on May 23, 2013