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Moyamoya Disease clinical trials

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NCT ID: NCT05332756 Recruiting - Moyamoya Disease Clinical Trials

Long-term Outcomes of Conservative Management in Patients With Moyamoya Disease and Their First-degree Relatives (LAMORA)

Start date: May 1, 2022
Phase:
Study type: Observational

The purpose of this study is to investigate the long-term outcomes of conservative management in patients with moyamoya disease and their first-degree relatives, and provide potential pathogenesis of moyamoya disease.

NCT ID: NCT05160454 Suspended - Moyamoya Clinical Trials

NIRS to Evaluate Haemodynamic Reserve in Paediatric Moyamoya

NIRS moyamoya
Start date: February 14, 2018
Phase: N/A
Study type: Interventional

Near infrared spectroscpy is a validated method of evaluating cerebral blood flow. The aim in this pilot study to explore its use in children with moyamoya disease.

NCT ID: NCT05050344 Recruiting - Moya Moya Disease Clinical Trials

Moya Moya Syndrome With or Withtout Sickle Cell Disease

BMM-ScD
Start date: May 1, 2021
Phase:
Study type: Observational

Moya Moya disease or syndrome ar characterized by a progressive or occlusion of the intracranial carotid arteries and their mainproximal branches, followed by the development of fragile neovessels at the base of the skull, leding to a high risk of both ischemic and hemorragic stroke over time. Moya Moya syndrome are associated to a variety of disease, which main frequent is sickle cell disease (SCD). Among patients with SCD who had suffered from at least one ischemic stroke, the prevalence of moya moya syndrome was estimated up to 43%. In general, therapeutic strategies in Moya Moya to prevent first ever ou recurrent stroke can be divided into conservative medical treatment and surgical revascularisation (direct bypass, indirect bypass or combined bypass). The aim of this study is to compare prognosis of patients with Moya Moya syndrome associated with sickle cell disease or not. The investigators retrospectiveluy analysed medical chart from 2010 to 2021 of patients with Moya Moya disease or syndrome at two French university hospitals (including a center of the french West Indies where prevalence of sickle cell disease is high). The diagnosis was based on angiography or MRI records showing uni- or bilateral stenosis of distal intracranial internal carotide arteries or middle cerebral arteries associated wirh classic collateral network. Main endpoint will be comparison of a composite outcome defined as time from Moya Moya diagnosis to first or recurrent stroke or bad prognosis achivement (defined by modified Rankin score >2)

NCT ID: NCT04917003 Recruiting - Moyamoya Disease Clinical Trials

Safety and Efficacy of Remote Ischemic Conditioning Combined EDAS on Ischemic Moyamoya Disease

RIC-IMD
Start date: June 15, 2021
Phase: N/A
Study type: Interventional

Encephaloduroarteriosynangiosis (EDAS) is widely used as an indirect technique for treatment of moyamoya disease. Nevertheless, this indirect surgery tends to establish insufficient collateral circulation in most adult MMD patients. Nowadays, there is a lack of adjuvant therapies for improving collateral circulation induced by indirect revascularization. This study aims to explore whether remote ischemic conditioning can improve the collateral circulation after indirect revascularization.

NCT ID: NCT04906564 Completed - Moyamoya Disease Clinical Trials

RNF213 Variants and Collateral Vessels in Moyamoya Disease

Start date: January 1, 2019
Phase:
Study type: Observational

The purpose of this study is to detect the association between RNF213 variants and collateral vessels in patients with moyamoya disease.

NCT ID: NCT04890782 Recruiting - Gut Microbiota Clinical Trials

Gut Microbiota in Patients With Moyamoya Disease

Start date: May 1, 2021
Phase:
Study type: Observational

This study is to find out the association between gut microbiota and moyamoya disease.

NCT ID: NCT04696094 Recruiting - Moyamoya Disease Clinical Trials

The Role of m6A RNA Modification in Moyamoya Disease

Start date: January 1, 2021
Phase:
Study type: Observational

The purpose of this study is to detect the change of m6A RNA modification from peripheral blood of patients with moyamoya disease, and to assess the relationship between clinical characteristics.

NCT ID: NCT04205578 Not yet recruiting - Ischemic Stroke Clinical Trials

NBP in Patients With Moyamoya Disease of High Risk for Ischemic Cerebrovascular Events

NICE-MMD
Start date: January 2020
Phase: Phase 3
Study type: Interventional

An extracranial-to-intracranial (EC-IC) revascularization is the most widely used treatment to improve cerebral perfusion in patients with moyamoya disease (MMD), and it has been shown to reduce the risk of subsequent stroke and neurological deficit. However, perioperative changes in cerebral hemodynamics can induce fluctuations in cerebral perfusion that may lead to transient or irreversible neurological deficits. Our preliminary single-center study suggests that postoperative intravenous administration of dl-3-n-butylphthalide (NBP) may alleviate perioperative neurological deficits and improve the neurological outcomes after EC-IC revascularization for MMD. This is a multicenter, randomized, double-blind, single-controlled, add-on to standard of care study of NBP in patients with MMD of high risk for ischemic cerebrovascular events after EC-IC revascularization surgery.

NCT ID: NCT04134221 Completed - Clinical trials for Carotid Artery, Internal

Internal Carotid Artery Blood Flow in Pediatric Moyamoya Patients

Start date: October 18, 2019
Phase:
Study type: Observational

Little is known about how general anesthesia-induced decrease in cerebral blood flow in pediatric moyamoya pateints. We investigated this question in patients undergoing moyamoya surgery, hypothesizing that cardiorespiratory changes during this procedure would reduce cerebral perfusion.

NCT ID: NCT04064658 Suspended - Moyamoya Disease Clinical Trials

Effects of Remote Ischemic Pre-Conditioning in Moyamoya Disease Patients

RIME
Start date: October 1, 2019
Phase: N/A
Study type: Interventional

In the present study, investigators evaluated whether RIPC reduce the major neurological complications in adult moyamoya disease patients undergoing encephaloduroarteriosynangiosis (EDAS).