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Study of the Metabolism of Pyruvate and Related Problems in Patients With Lactic Acidemia

This study has been completed.

Sponsors and Collaborators: National Center for Research Resources (NCRR)
University of California, San Diego
Information provided by: National Center for Research Resources (NCRR)
ClinicalTrials.gov Identifier: NCT00004353
  Purpose

OBJECTIVES: I. Study the metabolism of pyruvate and related problems in patients with lactic acidemia.

II. Define the nature of the metabolic defect.


Condition
Mitochondrial Myopathy
MELAS Syndrome
Lactic Acidosis

Genetics Home Reference related topics:   mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes    mitochondrial neurogastrointestinal encephalopathy disease   

MedlinePlus related topics:   Muscle Disorders   

U.S. FDA Resources

Study Type:   Observational

Further study details as provided by National Center for Research Resources (NCRR):

Estimated Enrollment:   35
Study Start Date:   December 1978

Detailed Description:

PROTOCOL OUTLINE: Patients fast for 6 hours. Glucagon IM is administered after the 6 hour fast. Glucose level is measured at 0, 15, 30, 45, 60, and 90 minutes.

In children of sufficient size, alanine and lactic acid should also be measured at each or most of these time points.

Fasting continues for at least 18 hours. Glucagon IM is administered again at end of fast. Glucose level is measured at time 0, 15, 30, 45, 60, and 90 minutes.

  Eligibility
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

PROTOCOL ENTRY CRITERIA:

  • Diagnostically documented elevation in lactate, pyruvate, and/or alanine levels in lactic acidemia patients
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00004353

Locations
United States, California
University of California San Diego Medical Center    
      San Diego, California, United States, 92103-8757

Sponsors and Collaborators
National Center for Research Resources (NCRR)
University of California, San Diego

Investigators
Study Chair:     Richard H. Haas     University of California, San Diego    
  More Information

Study ID Numbers:   NCRR-M01RR00827-0071, UCSD-071
First Received:   October 18, 1999
Last Updated:   July 9, 2008
ClinicalTrials.gov Identifier:   NCT00004353
Health Authority:   United States: Federal Government

Keywords provided by National Center for Research Resources (NCRR):
MELAS syndrome  
inborn errors of metabolism  
lactic acidosis  
mitochondrial myopathy  
rare disease  

Study placed in the following topic categories:
MELAS syndrome
Acidosis, Lactic
Metabolic Diseases
Rare Diseases
Central Nervous System Diseases
Mitochondrial Diseases
Brain Diseases
Acidosis
MELAS Syndrome
Metabolism, Inborn Errors
Muscular Diseases
Genetic Diseases, Inborn
Musculoskeletal Diseases
Neuromuscular Diseases
Mitochondrial Myopathies
Brain Diseases, Metabolic, Inborn
Metabolic disorder
Brain Diseases, Metabolic

Additional relevant MeSH terms:
Mitochondrial Encephalomyopathies
Pathologic Processes
Disease
Syndrome
Nervous System Diseases
Acid-Base Imbalance

ClinicalTrials.gov processed this record on September 04, 2008




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