Hybrid Operating Treatment of Coexistence of Intracranial Aneurysms and Cerebrovascular Stenosis

NCT03204435 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 196

Last updated 2017-07-02

No results posted yet for this study

Summary

To evaluate the clinical benefits and risks of hybrid operating techniques in management of intracranial aneurysms with coexistence of atherosclerotic intracranial arterial stenosis.

Conditions

  • Intracranial Aneurysm
  • Cerebrovascular Stenosis
  • Atheroscleroses, Cerebral

Interventions

PROCEDURE

Microsurgical aneurysmal operating techniques

The microsurgical techniques used to evacuate the aneurysm out of circulation or reduce its risk of rupture by aneurysmal clipping, wrapping,or isolation.

PROCEDURE

endovascular techniques for cerebrovascular stenosis

The endovascular techniques that recanalize the narrowed or occluded cerebrovascular, including stent implantation, balloon dilatation.

PROCEDURE

endovascular techniques for intracranial aneurysms

The endovascular techniques that embolize the cavity of aneurysms to reduce the risk of rupture, including coiling embolization, balloon-assisted occlusion.

PROCEDURE

carotid endarterectomy

A microsurgical technique to recanalize the stenosis or occluded proximal segment of carotid artery.

Sponsors & Collaborators

  • Beijing Municipal Science & Technology Commission

    collaborator OTHER
  • liuxingju

    lead OTHER_GOV

Principal Investigators

  • Jizong Zhao, MD · Beijing Tiantan Hospital

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2019-06-30
Completion
2019-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03204435 on ClinicalTrials.gov