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Decompressive Craniectomy Combined With Hematoma Removal to Treat ICH (CARICH)

Primary Purpose

Intracranial Hemorrhages

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Decompressive Craniectomy
non-Decompressive Craniectomy
Sponsored by
Southwest Hospital, China
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Intracranial Hemorrhages

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Evidence of a spontaneous lobar and basal ganglia ICH on CT scan
  • Patient within 72 hours of ictus
  • Best score on the GCS of 5-13.
  • Volume of hematoma between 30 and 100ml [Calculated using (a x b x c)/2 method]
  • The history of hypertensive

Exclusion Criteria:

  • Clear evidence that the hemorrhage is due to an aneurysm or angiographically proven arteriovenous malformation.
  • Intraventricular hemorrhage of any sort
  • ICH secondary to tumour or trauma.
  • If the hematological effects of any previous anticoagulants are not completely reversed.

Sites / Locations

  • Department of Neurosurgery , Southwest Hospital, Third Military Medical University,Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Decompressive Craniectomy

non-Decompressive Craniectomy

Arm Description

Decompressive Craniectomy afte Hematoma Removal in Patients with Intracerebral Hemorrhage

non-Decompressive Craniectomy afte Hematoma Removal in Patients with Intracerebral Hemorrhage

Outcomes

Primary Outcome Measures

Mortality and disability
according to a 3-6 scores on the modified Rankin Score

Secondary Outcome Measures

Occurrence of second Surgery

Full Information

First Posted
May 7, 2014
Last Updated
February 4, 2016
Sponsor
Southwest Hospital, China
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1. Study Identification

Unique Protocol Identification Number
NCT02135783
Brief Title
Decompressive Craniectomy Combined With Hematoma Removal to Treat ICH
Acronym
CARICH
Official Title
A Randomised Trial to Establish the Efficacy and Safety of Decompressive Craniectomy Combined With Hematoma Removal in Patients With Intracerebral Hemorrhage
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Unknown status
Study Start Date
October 2014 (undefined)
Primary Completion Date
October 2017 (Anticipated)
Study Completion Date
October 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Southwest Hospital, China

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Decompressive craniectomy has been reported for the treatment of patients with intracerebral hemorrhage. But no prospective randomised controlled trials have yet been undertaken to confirm its effect.The purpose of the study is to determine whether decompressive craniectomy post hematoma removal surgery after intracerebral hemorrhage will reduce the chances of a person dying or surviving with a long term disability.
Detailed Description
Intracerebral hemorrhage (ICH) is one of the most serious subtypes of stroke, affecting approximately 2-3 million people worldwide each year. About one third of people with ICH die early after onset and the majority of survivors are left with major long-term disability. Hematoma removal (HR) surgery is the primary treatment for ICH which volume is more than 30ml. But whether decompressive craniectomy (DC) should be employed during the HR surgery still has considerable controversy. Outcomes in this study will be measured at 3 months after surgery via a postal questionnaire including the Glasgow Outcome scale, Modified Rankin Scale, and Barthel index. Two hundred patients will be recruited to the trial over 36 months. Follow-up will take three months with analysis and reporting taking one year.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intracranial Hemorrhages

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Decompressive Craniectomy
Arm Type
Experimental
Arm Description
Decompressive Craniectomy afte Hematoma Removal in Patients with Intracerebral Hemorrhage
Arm Title
non-Decompressive Craniectomy
Arm Type
Active Comparator
Arm Description
non-Decompressive Craniectomy afte Hematoma Removal in Patients with Intracerebral Hemorrhage
Intervention Type
Procedure
Intervention Name(s)
Decompressive Craniectomy
Intervention Description
A portion of frontal,temporal, and parietal bone was removed by craniectomy and the size of decompression was about 10x12 cm2.Intracerebral hematoma was evacuated by transcortical approach with the aid of a surgical microscope.
Intervention Type
Procedure
Intervention Name(s)
non-Decompressive Craniectomy
Intervention Description
a simple hematoma removal by osteoplastic craniotomy group (HR) or Intracerebral hematoma was evacuated by transcortical approach with the aid of a surgical neuroendoscopyand the size of decompression was about 3x2.5 cm2.
Primary Outcome Measure Information:
Title
Mortality and disability
Description
according to a 3-6 scores on the modified Rankin Score
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Occurrence of second Surgery
Time Frame
72 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Evidence of a spontaneous lobar and basal ganglia ICH on CT scan Patient within 72 hours of ictus Best score on the GCS of 5-13. Volume of hematoma between 30 and 100ml [Calculated using (a x b x c)/2 method] The history of hypertensive Exclusion Criteria: Clear evidence that the hemorrhage is due to an aneurysm or angiographically proven arteriovenous malformation. Intraventricular hemorrhage of any sort ICH secondary to tumour or trauma. If the hematological effects of any previous anticoagulants are not completely reversed.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rong Hu, MD,PhD
Organizational Affiliation
Department of Neurosurgery, Southwest Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Neurosurgery , Southwest Hospital, Third Military Medical University,
City
Chongqing
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rong Hu, MD
Phone
+8615123917123
Email
huchrong@aliyun.com
First Name & Middle Initial & Last Name & Degree
Rong Hu, MD PHD

12. IPD Sharing Statement

Citations:
PubMed Identifier
32514905
Citation
Hu R, Zhang C, Xia J, Ge H, Zhong J, Fang X, Zou Y, Lan C, Li L, Feng H. Long-term Outcomes and Risk Factors Related to Hydrocephalus After Intracerebral Hemorrhage. Transl Stroke Res. 2021 Feb;12(1):31-38. doi: 10.1007/s12975-020-00823-y. Epub 2020 Jun 8.
Results Reference
derived

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Decompressive Craniectomy Combined With Hematoma Removal to Treat ICH

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