- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02026284
Factors Affecting Anesthesia Preferences of Gravid Women
Factors Affecting Anesthesia Preferences of Gravid Women Who Are to Deliver by Caesarean Section
The investigators aim to evaluate the preferences for anaesthesia methods of gravid women who are to deliver baby by caesarean section, the rates of general anaesthesia and regional anaesthesia, the reasons for preferences of general anaesthesia and regional anaesthesia and the factors affecting these preferences.
A questionnaire consisting of 20 questions were applied to gravid women applying for delivery by elective caesarean operation, at Ankara University Faculty of Medicine Hospital for Gynaecology and Obstetrics between February 2010 and February 2011, in order to study the anaesthesia technique the patients prefer and the reason behind their preferences. Those gravid women who accepted to take part in the study were provided information about the questionnaire and their oral and written approvals were obtained.
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Ankara, Turkey
- Ankara University Medical School Anesthesiology and ICU Department
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- gravid women who were between 26th and 40th week of their pregnancy were included in the questionnaire.
Exclusion Criteria:
- gravid women who were taken into emergency service, those with communication problems, those whose mental conditions deter them to answer questions and those who did not want to answer the questions on the questionnaire
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Gravid women
A questionnaire was performed to gravid women
|
A questionnaire was performed to gravid women who are to deliver, regarding theri anesthesia preferences.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Percentage of participants who prefer regional anesthesia and who prefer general anesthesia
Time Frame: 1 day
|
1 day
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Factors affecting the preference of regional anesthesia and general anesthesia
Time Frame: 1 day
|
1 day
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Helin Sahintürk, Specialist, Ankara University Medical School Anesthesiology and ICU
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 38-828
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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