Study of the Metabolism of Pyruvate and Related Problems in Patients With Lactic Acidemia
This study has been completed.
Sponsor:
Collaborator:
University of California, San Diego
Information provided by:
National Center for Research Resources (NCRR)
ClinicalTrials.gov Identifier:
NCT00004353
First received: October 18, 1999
Last updated: July 9, 2008
Last verified: April 2002
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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 |
| Study Type: | Observational |
Resource links provided by NLM:
Genetics Home Reference related topics:
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childhood myocerebrohepatopathy spectrum
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mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
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succinic semialdehyde dehydrogenase deficiency
MedlinePlus related topics:
Muscle Disorders
U.S. FDA Resources
Further study details as provided by National Center for Research Resources (NCRR):
| Estimated Enrollment: | 35 |
| Study Start Date: | December 1978 |
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
University of California, San Diego
Investigators
| Study Chair: | Richard H. Haas | University of California, San Diego |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00004353 History of Changes |
| Other Study ID Numbers: | NCRR-M01RR00827-0071, UCSD-071 |
| Study First Received: | October 18, 1999 |
| Last Updated: | July 9, 2008 |
| 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 |
Additional relevant MeSH terms:
|
Acidosis Acidosis, Lactic Muscular Diseases Mitochondrial Myopathies MELAS Syndrome Acid-Base Imbalance Metabolic Diseases Musculoskeletal Diseases Neuromuscular Diseases |
Nervous System Diseases Mitochondrial Diseases Mitochondrial Encephalomyopathies Brain Diseases, Metabolic, Inborn Brain Diseases, Metabolic Brain Diseases Central Nervous System Diseases Metabolism, Inborn Errors Genetic Diseases, Inborn |
ClinicalTrials.gov processed this record on May 23, 2013