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NCT03447327 Clinical Trial

Outcome of Single Burr Hole Under Local Anaesthesia in the Management of Chronic Subdural Hematoma

Chronic Subdural Hematoma Clinical Trial

Official title:
Outcome of Single Burr Hole Under Local Anaesthesia in the Management of Chronic Subdural Hematoma

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03447327
Other study ID # ZU-IRB#3893-03-03-2014
Secondary ID
Status Completed
Phase N/A
First received February 20, 2018
Last updated February 25, 2018
Start date March 5, 2014
Est. completion date August 28, 2015

Study information
Verified date February 2018
Source Zagazig University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aim of the work: Is to evaluate the prognosis of single burr hole under local anesthesia in management of CSDH according to clinical picture, risk factors, and age.

Description:

Patients and methods: We studied 67 consecutive patients with CSDH operated by single burr hole craniostomy under local anaesthesia from Mars, 2014 to February, 2015 in Zagazig University Hospitals according to the aetiology, clinical picture, risk factors, and complications.

Recruitment information / eligibility
Status Completed
Enrollment 67
Est. completion date August 28, 2015
Est. primary completion date February 28, 2015
Accepts healthy volunteers No
Gender All
Age group 19 Years to 90 Years
Eligibility Inclusion Criteria:chronic subdural hematoma above 19 years old -

Exclusion Criteria:age below 19 years acute subduralhematoma uncoperative patients

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• single burr hole
patients with CSDH operated by single burr hole craniostomy under local anaesthesia

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Zagazig University

Outcome
Type Measure Description Time frame Safety issue
Primary Glasgow Outcome Scale The Glasgow Outcome Scale was used as measuremabilityent for neurological oucome after surgery.The patients were classified as as dead, persistant vegetative state, severe disability, moderate disability, and mild dis 6 months postoperative
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