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CompletedNCT04287881Updated Feb 27, 2020

Methylenetetrahydrofolate Reductase Deficiency in Ischemic Stroke

An interventional study of Methylenetetrahydrofolate reductase (MTHFR) deficiency in Hyperhomocysteinemia, Thrombotic, Cbs-Related, Ischemic Stroke and Epilepsy, sponsored by Istanbul Medeniyet University. Completed at 2 sites in Turkey. Per ClinicalTrials.gov, last updated 2020-02-27.

Sponsored by Istanbul Medeniyet University · Not applicable, Interventional, and Screening

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Oct 2019, registered Feb 2020).
Phase
Not applicable
Study type
Interventional
Enrollment
32
Allocation
Not applicable
Sex
All
01

Study summary

Adult onset epileptic seizures is rare and often associated with metabolic disorders, drugs and intracranial pathologies such as ischemia, hemorrhage or space-occupying lesions. Methylenetetrahydrofolate reductase (MTHFR) deficiency is one of the reasons that cause epileptic seizures in adults and can be ignored. MTHFR deficiency is an autosomal recessive disorder that results in hyperhomocysteinemia and causes a predisposition to venous and arterial thrombosis. The incidence of the polymorphism is around 40% in some countries. The aim of the retrospective study is to investigate the incidence of MTHFR deficiency in patients with adult-onset epileptic seizures.

Read the detailed description

Epileptic seizures that begin in adulthood seriously affect patients, their relatives and the society in which they live financially and psychologically. The etiology of epileptic seizures starting at adult age includes head trauma, central nervous system infections, intracranial lesions, cerebrovascular events, metabolic diseases and drugs. While the causes of childhood epileptic seizures are generally considered idiopathic, adult-onset epileptic seizures are almost always due to a pathological process. Epileptic seizures in adults may be a symptom of ischemic stroke. MTHFR deficiency is associated with raised homocysteine concentration in the body and increased risk of stroke (1). Studies have demonstrated that hyperhomocysteinemia is an independent risk factor for stroke (2).

MTHFR is the key enzyme in remethylation of homocysteine to methionine. MTHFR deficiency is an autosomal-recessive disease characterized by high homocysteine and low or normal methionine. MTHFR deficiency can cause vascular thrombosis in adults at early age; increased osteoporosis in elderly people; deep vein thrombosis, abortus during pregnancy; and infertility in adult males. In children, it is associated with intrauterine growth retardation, congenital heart diseases, neural tube defects, chromosome anomalies and hematologic tumors. In any age group, it might cause convulsions, increased thrombosis risk with some anticonvulsants and with the use of nitrogen protoxide in surgeries, and neuromotor retardation (3).

The aim of this retrospective study is to investigate the incidence of MTHFR deficiency in patients presenting with adult-onset epileptic seizures and diagnosed as ischemic cerebrovascular disease as a result of diagnostic tests.

02

Conditions studied

  • Hyperhomocysteinemia, Thrombotic, Cbs-Related
  • Ischemic Stroke
  • Epilepsy

Keywords

  • Methylenetetrahydrofolate reductase (MTHFR) deficiency
  • Ischemic Stroke
  • Epileptic seizures
  • Adult patients
03

In context

Hyperhomocysteinemia

34 studies on the registry are indexed under Hyperhomocysteinemia; 4 are open to participants now.

This study's enrollment of 32 is below the median of 84 across 21 interventional studies indexed under Hyperhomocysteinemia.

Browse Hyperhomocysteinemia studies →

Lead sponsor

Istanbul Medeniyet University is the lead sponsor of 192 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • The patients with adult-onset epileptic seizures and diagnosed ischemic stroke in 3 years period.

Exclusion criteria

Exclusion Criteria:

  • Pediatric patients with epileptic seizures
05

Study design

Phase
Not applicable
Primary purpose
Screening
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
32 participants (actual)

Study arms

  • Other
    Adult patients who have epileptic seizures

    Patients with adult-onset epileptic seizures and diagnosed ischemic stroke.

    Genetic: Methylenetetrahydrofolate reductase (MTHFR) deficiency

Interventions

  • GeneticMethylenetetrahydrofolate reductase (MTHFR) deficiency

    To investigate the incidence of MTHFR deficiency in patients with adult-onset epileptic seizures and diagnosed ischemic stroke

06

What researchers measure

Primary outcomes

  1. Methylenetetrahydrofolate reductase (MTHFR) deficiency

    The incidence of methylenetetrahydrofolate reductase (MTHFR) deficiency in ischemic stroke

    Time frame: Up to 6 weeks

07

Study locations

2 sites
  • Zeynep Orhon
    İstanbul, 34722, Turkey
  • Istanbul MU Goztepe Training and Research Hospital
    Istanbul, 34730, Turkey
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Oct 2019 to primary completion in Feb 2020, 3 months.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 22, 2020
First posted
Feb 27, 2020
StartActual
Oct 31, 2019
Primary completionActual
Feb 15, 2020
CompletionActual
Feb 20, 2020
Last update
Feb 27, 2020
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 27, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04287881
Responsible party
Zeynep Nur Orhon (Principal Investigator, Istanbul Medeniyet University) — Principal investigator
First posted
Feb 27, 2020
Start date
Oct 31, 2019
Primary completion
Feb 15, 2020
Completion
Feb 20, 2020
Last update
Feb 27, 2020

Study contacts

ZEYNEP ORHON, MD
principal investigator · Istanbul Medeniyet University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2020. You cannot join it, but the record below documents what was studied.

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