Sodium Lactate Infusion in GLUT1DS Patients

NCT ID: NCT04112862

Last Updated: 2022-11-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

EARLY_PHASE1

Total Enrollment

2 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-05-20

Study Completion Date

2022-11-18

Brief Summary

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This study investigates the effect of lactate infusion on epileptic discharges on EEG and seizure frequency in glucose transporter 1 deficiency syndrome (GLUT1DS) patients.

Detailed Description

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In glucose transporter 1 deficiency syndrome (GLUT1DS) cerebral glucose uptake from the systemic blood circulation is limited, because of deficient transport of glucose across the blood-brain barrier by the transporter protein (GLUT1). Classically patients present with developmental problems, movement disorders and severe epilepsy. There is no curative treatment for GLUT1DS, and anti-epileptic drugs usually have little to no effect. The ketogenic diet, providing ketones as an alternative energy substrate for the brain is an effective treatment option for the epilepsy and movement disorders in many GLUT1DS patients. Unfortunately, not in all GLUT1DS patients the ketogenic diet has a positive effect and other treatment options for these patients are very limited.

Traditionally, lactate is seen as a waste product of glycolysis during anaerobic conditions and a marker of ischemia. Interestingly, research has shown the beneficial side of lactate as an energy source for different organs. It seems that the brain can indeed use lactate as an alternative energy metabolite, besides glucose and ketones. The aim of this study is to investigate whether lactate can be an alternative energy metabolite in the GLUT1DS brain, and reduce epileptic discharges on EEG when intravenously administered in patients with GLUT1DS.

Conditions

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GLUT1 Deficiency Syndrome GLUT1DS1 GLUT1DS2 Epilepsy Lactic Acid Blood Increased Ketogenic Dieting

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Single center, interventional, explorative, open label, proof of principle study
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Intervention

three GLUT1DS patients with drug resistant epilepsy who tried the ketogenic diet without any benefits.

Group Type EXPERIMENTAL

sodiumlactate

Intervention Type OTHER

intravenous sodiumlactate 600mmol/L

Interventions

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sodiumlactate

intravenous sodiumlactate 600mmol/L

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Diagnosed with GLUT1DS and known in our center.
* Baseline characteristics include a high frequency of clinical seizures and epileptic discharges on EEG.
* History of trying ketogenic diet with good compliance without beneficial effects.
* Age \> 6 years.
* Informed consent.

Exclusion Criteria

* Additional medical condition or illness that impairs the patient's ability to participate in the study (for example actual treatment of a malignancy, active infection, poorly controlled diabetes mellitus, hypertension, organ failure, clinically significant haematological or biochemical abnormalities).
* Elevated serum sodium (\> 145 mmol/L).
* Participation in another interventional study at start of the study or during the study.
* Presence of known panic disorders or a history of panic attacks.
Minimum Eligible Age

6 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Radboud University Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Radboudumc

Nijmegen, Gelderland, Netherlands

Site Status

Countries

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Netherlands

Other Identifiers

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109147

Identifier Type: -

Identifier Source: org_study_id

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