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NCT Number: NCT06013397

Effectiveness of Ketogenic Diet in MELAS Syndrome

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

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Key information

About this study

Ketogenic diet initiation and follow-up:

  • Before starting ketogenic diet treatment, patients with abnormal indexes such as liver, kidney, lipid, humoral immunity, hematuria, routine biochemical, electrolyte, trace elements and bone metabolism should be excluded, energy and nutrients should be calculated according to their height and weight, and patients will be taught with ketogenic diet treatment education
  • Patients were initiated ketogenic diet after a short period of fasting (fasting no more than 48 hours). After treatment was initiated, 13 of the calculated target energy was given on the first day, 23 of the target energy was given on the second day, and the target amount was reached on the third day. Nutritionists made appropriate adjustments to the target energy according to the level of blood keto measured by patients
  • Weekly follow-up via telemedicine system or social media, outpatient follow-up at the initiation of ketogenic therapy and at 1 month, 3 months, 6 months, and 12 months respectively. Outpatient follow-up was done in a joint clinic with a dietitian and a neurologist to evaluate the effects and side effects of ketogenic therapy on a compliant diet and related clinical examinations

Clinical data collection:

  • Demographic information and Medical history collection Gender, age, education level age of onset, genetic test, drug use, past history, personal history, family history
  • Clinical symptom collection According to the Newcastle Mitochondrial Disease Adult Scale(NMDAS), including migraine headaches, seizures, stroke-like episodes and etc.
  • Biochemical indicators Blood glucose, keto, lactate and pyruvate monitoring, dietary status, dietary ratio changes, energy changes, weight changes
  • Cognitive function assessment Cognitive function was assessed using Fepsy software
  • Diagnostic Examination Cranial MRI, scalp EEG

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients who meet the diagnostic criteria of MELAS and have received MELAS standard therapy but are not satisfied with the therapeutic effect, and voluntarily underwent ketogenic therapy

Exclusion criteria

  • Diseases with porphyria and disturbances in fatty acid transport and oxidation, severe electrolyte metabolism abnormalities, severe hemodynamic instability, acute respiratory infections, uncontrolled systemic infections, severe liver and renal failure, cholesterolemia (>300mgdl), abnormal coagulation, acute pancreatitis, eating disorders, ketogenic diet intolerance, significant weight loss, poor compliance

Treatment and study plan

Ketogenic diet

Dietary Supplement

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.

Primary outcomes

  1. Change from Baseline Clinical Symptom Score in 1 Year

    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.

  2. Change from Baseline Biochemical indicators in 1 Year

    Time frame: Baseline, 1 month, 3 months, 6 months and 12 months

    Blood glucose

  3. Change from Baseline Biochemical indicators in 1 Year

    Time frame: Baseline, 1 month, 3 months, 6 months and 12 months

    keto, lactate and pyruvate monitoring

  4. Hamilton Anxiety Scale (HAMA)

    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

  5. Hamilton Depression Scale(HAMD

    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

  6. Wechsler Intelligence Scale(WISC)

    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

  7. Mini-mental State Examination(MMSE)

    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

  8. Change from Baseline Diagnostic Examination in 1 Year

    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

Secondary outcomes

  1. Demographic Information and Medical History Collection

    Time frame: Baseline

    Gender, age, education level age of onset, genetic test, drug use, past history, personal history, family history

Study contacts

Contact information is provided by the study sponsor or research team.

Yao Ding, doctor

CONTACT

[email protected]

13588015954

Sponsors and collaborators

Lead sponsor

Second Affiliated Hospital, School of Medicine, Zhejiang University

Other

Registry information

Official study title

Clinical Trial of Ketogenic Diet in the Treatment of Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-like Episodes(MELAS)

Important dates

Study start
2023
Primary completion
2038
Study completion
2038
First posted
Aug 28, 2023
Registry last updated
Aug 28, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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