SMAVMHR: Surgical Management of Cerebral Arteriovenous Malformations Within Hybrid Operation Room

Sponsor
Ministry of Science and Technology of the People´s Republic of China (Other)
Overall Status
Completed
CT.gov ID
NCT03209804
Collaborator
Beijing Municipal Science & Technology Commission (Other)
519
4
2
43.5
129.8
3

Study Details

Study Description

Brief Summary

To evaluate the clinical benefits and risks of hybrid operating techniques in management of cerebral arteriovenous malformations.

Condition or Disease Intervention/Treatment Phase
  • Procedure: hybrid operating techniques
N/A

Detailed Description

Purpose: Have an evaluation of clinical benefits and risks of hybrid operating techniques in management of cerebral arteriovenous malformations(AVMs). Meanwhile, as a new cooperative interventional modality, optimized workflows, technical key knots and operation routines will be explored in the study.

Objects: Patients with cerebral arteriovenous malformations, coincident with inclusion and exclusion criterion and admitted in participating organizations.

Methods: Patients will be distributed into 2 groups, including traditional therapy group(control group) and hybrid operating group(trial group), and conduct with traditional neurosurgical management or one-stage hybrid operating management correspondingly. Residual rate of AVM is considered to be the primary observing indicator, and morbidity rate of post-operative complications, post-operative mortality rate, and morbidity rate of neural functional deterioration are secondary indicators.The information of operations will be recorded in detail as evidence of optimization of workflow and technical key knots.

Study Design

Study Type:
Interventional
Actual Enrollment :
519 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Traditional therapy group:traditional management of AVMs, such as unsimultaneous endovascular interventional embolisation, radiotherapy followed by microsurgical resection, will be conducted to patients involved in this group. Hybrid operation group: A one-stage hybrid operation combining endovascular intervention and microsurgical techniques will be conducted simultaneously to patients in this group.Traditional therapy group:traditional management of AVMs, such as unsimultaneous endovascular interventional embolisation, radiotherapy followed by microsurgical resection, will be conducted to patients involved in this group. Hybrid operation group: A one-stage hybrid operation combining endovascular intervention and microsurgical techniques will be conducted simultaneously to patients in this group.
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Surgical Management of Cerebral Arteriovenous Malformations Within Hybrid Operation Room
Study Start Date :
Jun 1, 2016
Actual Primary Completion Date :
Dec 1, 2019
Actual Study Completion Date :
Jan 16, 2020

Arms and Interventions

Arm Intervention/Treatment
Other: Traditional neurosurgical techniques

Unsimultaneous endovascular interventional embolisation/radiotherapy followed by microsurgical resection, as traditional clinical routines.

Procedure: hybrid operating techniques
A one-stage cooperation of existing endovascular interventional techniques and microsurgical techniques, including microsurgical resection, endovascular embolization, balloon occlusion.
Other Names:
  • endovascular interventional embolisation
  • endovascular interventional balloon occlusion
  • microsurgical resection
  • Experimental: Hybrid operating techniques

    A one-stage hybrid operation combining endovascular intervention and microsurgical techniques will be conducted simultaneously

    Procedure: hybrid operating techniques
    A one-stage cooperation of existing endovascular interventional techniques and microsurgical techniques, including microsurgical resection, endovascular embolization, balloon occlusion.
    Other Names:
  • endovascular interventional embolisation
  • endovascular interventional balloon occlusion
  • microsurgical resection
  • Outcome Measures

    Primary Outcome Measures

    1. Instant residual rate of AVMs [up to 1 week after operation]

      The instant post-operative residual rate of AVMs

    2. 3 months' residual rate of AVMs [the date of 3rd month after operation, ±1 week]

      3 months' residual rate after AVM operation

    3. 6 months' residual rate of AVMs [the date of the 6th month after operation, ±1 week]

      6 months' residual rate after AVM operation

    4. 1 year's residual rate of AVMs [the date of the 12th month after operation, ±1 week]

      1 year's residual rate after AVM operation

    Secondary Outcome Measures

    1. Morbidity rate of post-operative complications [7 days after operation]

      Include intracranial hemorrhage or infarction, infection of central neural system, infection of respiratory system, cranial nerve deficits, and other symptomatic complications

    2. Post-operative mortality rate [48 hours after operation]

      operation related mortality

    3. Morbidity rate of neural functional deterioration-48 hours after operation [the assessing time points is 48 hours after operation]

      The score of modified Rankin Scale increases ≥2

    4. Morbidity rate of neural functional deterioration-1 week after operation [1 week after operation]

      The score of modified Rankin Scale increases ≥2

    5. Morbidity rate of neural functional deterioration-3 months after operation [the 3rd month after operation, ±1 week]

      The score of modified Rankin Scale increases ≥2

    6. Morbidity rate of neural functional deterioration-6 months after operation [the 6th month after operation, ±1 week]

      The score of modified Rankin Scale increases ≥2

    7. Morbidity rate of neural functional deterioration-12 months after operation [the 12th month after operation, ±1 week]

      The score of modified Rankin Scale increases ≥2

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • newly ruptured AVM with stable hematoma, selective operation is practical;

    • with rupture history;

    • recurrent epilepsy, failed in AED management;

    • giant AVM with deterioration of neurological functions;

    • 1-4 grade AVM (Spetzler-Martin grading system) with no symptom and not located in eloquent area.

    Exclusion Criteria:
    • 70 in age, with low rupture risk;

    • newly ruptured AVM with unstable hematoma, engaged in emergency operation;

    • ≥5 grade in Spetzler-Martin grading system;

    • AVM located in hypothalamus, brainstem, cerebellopontine angle;

    • cannot tolerant the operation;

    • patient or relative refuses to participate the trail.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Beijing Tiantan Hospital Capital Medical University Beijing Beijing China 0086
    2 General Hospital of PLA Beijing Beijing China 100039
    3 Rocket Army General Hospital of PLA Beijing Beijing China 100088
    4 Beijing Hospital Beijing Beijing China 100730

    Sponsors and Collaborators

    • Ministry of Science and Technology of the People´s Republic of China
    • Beijing Municipal Science & Technology Commission

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Shuo Wang, liuxingju, Beijing Tiantan Hospital
    ClinicalTrials.gov Identifier:
    NCT03209804
    Other Study ID Numbers:
    • BJTTH-002
    First Posted:
    Jul 6, 2017
    Last Update Posted:
    Mar 13, 2020
    Last Verified:
    Mar 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Keywords provided by Shuo Wang, liuxingju, Beijing Tiantan Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 13, 2020