Second Affiliated Hospital, School of Medicine, Zhejiang University
Hangzhou, Zhejiang, 310000, China
NCT Number: NCT06013397
The goal of this clinical trial is to evaluate the effectiveness of ketogenic diet in patients with MELAS syndrome. The main questions it aims to answer are:
Clarify the curative effects of ketogenic diet in the treatment of MELAS disease.
Prevent the aggravation of MELAS disease, and improve the quality of life of patients.
Provide reliable evidence-based medical basis for the clinical application of ketogenic diet in the treatment of MELAS syndrome patients.
The clinical data of the participants treated with ketogenic diet will be collected, including the completion of ketogenic diet and clinical data at the start of treatment and after 1 month, 3 months, 6 months and 12 months
Trial opening soon.
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Interventional
Not applicable
Hangzhou, Zhejiang, 310000, China
Ketogenic diet initiation and follow-up:
Clinical data collection:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Ketogenic diet (KD) is a high-fat, low-carbohydrate and moderate protein diet pattern, suitable for refractory epilepsy, glucose carrier protein 1 deficiency, pyruvate dehydrogenase deficiency, tumors and some genetic metabolic diseases. The ketogenic diet has been used to treat epilepsy for nearly 100 years, and its safety has been recognized by the medical community. In 2015, the ketogenic diet was included in the "Clinical Diagnosis and Treatment Guidelines - Epilepsy Volume" and became a commonly used treatment for refractory epilepsy.
Time frame: Baseline, 1 month, 3 months, 6 months and 12 months
According to the newcastle mitochondrial disease adult scale(NMDAS), including migraine headaches, seizures, stroke-like episodes and etc.
Time frame: Baseline, 1 month, 3 months, 6 months and 12 months
Blood glucose
Time frame: Baseline, 1 month, 3 months, 6 months and 12 months
keto, lactate and pyruvate monitoring
Time frame: Baseline, 1 month, 3 months, 6 months and 12 months
Change from Baseline Cognitive Function in 1 Year. Cognitive function was assessed using "Fepsy" software
Time frame: Baseline, 1 month, 3 months, 6 months and 12 months
Change from Baseline Cognitive Function in 1 Year . Cognitive function was assessed using "Fepsy" software
Time frame: Baseline, 1 month, 3 months, 6 months and 12 months
Change from Baseline Cognitive Function in 1 Year . Cognitive function was assessed using "Fepsy" software
Time frame: Baseline, 1 month, 3 months, 6 months and 12 months
Change from Baseline Cognitive Function in 1 Year . Cognitive function was assessed using "Fepsy" software
Time frame: Baseline, 1 month, 3 months, 6 months and 12 months
Cranial MRI(multimodal) Scalp EEG to evaluate posterior head α rhythm, discharge index, interictal epileptic discharges
Time frame: Baseline
Gender, age, education level age of onset, genetic test, drug use, past history, personal history, family history
Contact information is provided by the study sponsor or research team.
Second Affiliated Hospital, School of Medicine, Zhejiang University
Other
Clinical Trial of Ketogenic Diet in the Treatment of Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-like Episodes(MELAS)
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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