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NCT04076449Recruiting

Quantitative Susceptibility Biomarker and Brain Structural Property for Cerebral Cavernous Malformation Related Epilepsy

Quantitative Susceptibility Mapping Biomarker, Brain Structure and Connectome Associated With Cerebral Cavernous Malformation Related Epilepsy and Outcome After Surgery

Source: ClinicalTrials.gov · Last updated 4 Sept 2019 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Cerebral cavernous malformation (CCM)-related epilepsy (CRE) impairs the quality of life in patients with CCM. Patients could not always achieve seizure freedom after surgical resection of the lesion, suggesting an inadequate treatment and evaluation of the epileptogenic zone or network. Iron deposition in cerebral cavernous malformations has been postulated to play an important role in triggering CRE. Quantitative susceptibility mapping (QSM), as an optimal in vivo imaging technique to quantify iron deposition, is employed to analyze the iron quantity in CCM patients with epilepsy and further combined with brain structural and connectome analysis, to describe the difference between CCMs with and without epilepsy. In vivo biomarkers predicting CRE risk in CCM natural history and CRE control outcome after CCM surgical resection will be further identified to improve management strategy.

Status (registry)
Recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
29 Aug 2019
Start date
3 Sept 2019
Primary completion date
31 Dec 2026
Lead sponsor
yuanli Zhao
Diseases
Epilepsy
NCT number
NCT04076449

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 3 Sept 2019 to the primary completion date, 31 Dec 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • (2) History of previous intracranial surgery
  • (3) Prior brain irradiation

Other illness

  • (7) Dementia or other progressive neurological disease

Other

  • (1) Associated with brain lesions and/or tumors other than CCM
  • (4) Contraindication or unwilling or unable to undergo research MRI studies
  • (5) Pregnant or breastfeeding women
  • (6) Persons unable or unlikely to return for follow-up visits

Who the study is looking for

  • (1) 18 to 70 years of age
  • (2) Diagnosed with a single cerebral cavernous malformation
  • (3) No prior treatment of the symptomatic lesion

Age in the registry: 18 years to 70 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Beijing Tiantan Hospital,Capital Medical University
Coordinator of this site? Confirm its status
BeijingChinaRecruiting
Peking University International Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.