- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01806155
Prevalence of Post-craniotomy Headache in Siriraj Hospital
August 16, 2013 updated by: Sirilak Suksompong, Mahidol University
Headache after major craniotomy may be a problem in taking care of the patients.
The investigators want to identify the incidence of headache after major craniotomy and also the risk factors.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Sirilak Suksompong, MD
- Phone Number: 6624113256
- Email: sirilak.suk@mahidol.ac.th
Study Locations
-
-
-
Bangkok, Thailand, 10700
- Recruiting
- Faculty of medicine, Siriraj hospital, Mahidol university
-
Contact:
- Sirilak Suksompong, MD
- Phone Number: 6624113256
- Email: sirilak.suk@mahidol.ac.th
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patient undergoing major craniotomy
Description
Inclusion Criteria:
- Patient undergoing major craniotomy
Exclusion Criteria:
- emergency surgery or traumatic patients
- may need postoperative ventilatory support more than 2 days
- cannot communicate
- psychiatric patients
- chronic use of benzodiazepine or drug abuse
- cannot follow the treatment
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
Craniotomy
Patient undergoing major craniotomy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The incidence of headache after major craniotomy
Time Frame: 3 months
|
By asking the patients about the symptoms
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
risk factors of headache after major craniotomy such as sex, education
Time Frame: 3 months
|
by collecting the patients data
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2013
Primary Completion (Anticipated)
March 1, 2014
Study Completion (Anticipated)
October 1, 2014
Study Registration Dates
First Submitted
March 3, 2013
First Submitted That Met QC Criteria
March 6, 2013
First Posted (Estimate)
March 7, 2013
Study Record Updates
Last Update Posted (Estimate)
August 19, 2013
Last Update Submitted That Met QC Criteria
August 16, 2013
Last Verified
August 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 734/2555(EC2)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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