Nitric Oxide Production in MELAS Syndrome

The recruitment status of this study is unknown because the information has not been verified recently.
Verified April 2011 by Baylor College of Medicine.
Recruitment status was  Recruiting
Information provided by:
Baylor College of Medicine Identifier:
First received: April 19, 2011
Last updated: NA
Last verified: April 2011
History: No changes posted


Baylor College of Medicine and Texas Children's Hospital are recruiting individuals with MELAS syndrome for a clinical study. Mitochondria are cell structures that provide energy for most cells of the body. MELAS syndrome is a mitochondrial disease; patients with this disease have muscle weakness and often develop brain strokes, where blood does not flow normally to different parts of the brain. It is believed that these strokes could be due to decreased production of nitric oxide, a naturally occurring compound important for normal blood vessel function. Nitric oxide is made from other common compounds arginine and citrulline that are normally found in our bodies.

What is the purpose of this study? The purpose of this study is to measure nitric oxide in individuals with MELAS syndrome and see if giving arginine or citrulline will increase the formation of nitric oxide. Nitric oxide is thought to be helpful in improving blood vessel function and preventing strokes. Therefore, if arginine and/or citrulline are shown to increase the formation of nitric oxide, they could be used to prevent or treat the strokes in patients with MELAS syndrome.

What does the study involve? Individuals with MELAS syndrome will be admitted twice to the General Clinical Research Center (GCRC) at Texas Children's Hospital. Each time they will stay for five days, during which a special diet will be provided. Nitric oxide production will be measured by a safe stable isotopes infusion technique that involves placing small tubes in veins (IV catheter), blood sampling, and injecting a harmless stable isotope. Stable isotopes are forms of normal compounds that can be measured very accurately but not radioactive and there are no known risks to giving them; they are already part of your body in small amounts.

During the first admission nitric oxide levels will be measured, then arginine supplementation will be provided for 48 hours, after which nitric oxide levels will be re-measured to determine the effect of arginine supplementation. During the second admission, the effect of citrulline supplementation will be measured.

Who can participate in the study? Adults or children affected with MELAS syndrome and carrying the DNA change that causes the condition (3243 A>G mutation) can participate. Adults without MELAS disease will be recruited to participate as control subjects.

How to get more information? Subjects interested in participation or getting more information can contact Dr. Ayman El-Hattab at email:, office phone: 832-822-4289, cell phone: 646-660-5666, or pager: 832-824-7243 (5523).

Condition Intervention
MELAS Syndrome
Dietary Supplement: Arginine and citrulline supplementations

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment

Resource links provided by NLM:

Further study details as provided by Baylor College of Medicine:

Primary Outcome Measures:
  • Change in nitric oxide production [ Time Frame: Nitric oxide production will be measured at baseline before supplementation and after 48 hours of arginine or citrulline supplementation ] [ Designated as safety issue: No ]

Estimated Enrollment: 10
Study Start Date: July 2009
Estimated Primary Completion Date: June 2012 (Final data collection date for primary outcome measure)
Intervention Details:
    Dietary Supplement: Arginine and citrulline supplementations
    Arginine or citrulline will be given orally at dose of 10 grams per meter square body surface area per day divided every 4 hours.

Ages Eligible for Study:   3 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  1. Age from 3 - 65 years
  2. Clinical diagnosis of MELAS syndrome
  3. Carrying the m.3243A>G mutation

Exclusion Criteria:

  1. Having acute or chronic disease or physical disability that will interfere with the ability to undergo the study procedures
  2. Being pregnant
  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 identifier: NCT01339494

Contact: Ayman W El-Hattab, M.D. 832-822-4289

United States, Texas
Texas Children's Hospital Recruiting
Houston, Texas, United States, 77030
Contact: Ayman W El-Hattab, MD    832-822-4289   
Principal Investigator: Fernando Scaglia, MD         
Sponsors and Collaborators
Baylor College of Medicine
Principal Investigator: Fernando Scaglia, M.D. Baylor College of Medicine
  More Information

No publications provided

Responsible Party: Fernando Scaglia, Baylor College of Medicine Identifier: NCT01339494     History of Changes
Other Study ID Numbers: H-24783
Study First Received: April 19, 2011
Last Updated: April 19, 2011
Health Authority: United States: Institutional Review Board

Additional relevant MeSH terms:
Mitochondrial Diseases
Mitochondrial Encephalomyopathies
Mitochondrial Myopathies
Muscular Diseases
MELAS Syndrome
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Cardiovascular Diseases
Central Nervous System Diseases
Cerebral Small Vessel Diseases
Cerebrovascular Disorders
Genetic Diseases, Inborn
Metabolic Diseases
Metabolism, Inborn Errors
Musculoskeletal Diseases
Nervous System Diseases
Neuromuscular Diseases
Vascular Diseases processed this record on March 26, 2015