- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02727244
The Association Between Pain Catastrophizing Scale Score and Postspinal Headache
June 16, 2018 updated by: Mustafa Suren, Tokat Gaziosmanpasa University
Is There an Association Between Pain Catastrophizing Scale Score and Postspinal Headache in Patients Underwent Cesarean Section With Spinal Anesthesia?
This study is aimed to elucidate the association between Pain Catastrophizing Scale Score and Postspinal Headache in Patients Underwent Cesarean Section With Spinal Anesthesia.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
This study is aimed to elucidate the association between Pain Catastrophizing Scale Score and Postspinal Headache in Patients Underwent Cesarean Section With Spinal Anesthesia.
Patients were asked to fill the questionnaire booklet including Pain Catastrophizing Scale, Beck Depression Inventory and Beck Anxiety Inventory before elective cesarean section in preoperative room in operating theater.
In postoperative second and fourth day, patients will call by phone and be asked to have headache or any complaints.
The intensity of headache will evaluate by using visual analog scale.
Age, gender, and visual analog scale scores will be recorded.
Study Type
Observational
Enrollment (Actual)
300
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 to 40 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Probability Sample
Study Population
women with pregnancy whose planned to undergo urgent or elective cesarean section
Description
Inclusion Criteria:
- American Society of Anesthesiologists score of I, II, III
- without a history of cerebrovascular diseases
- without any presence of psychiatric diseases
Exclusion Criteria:
- severe liver, kidney and cardiovascular diseases
- peripheral arterial diseases
- a history of allergy to local anesthetics
- patients without cooperation
- not to participate in the study
- presence of neurologic or neuromuscular diseases
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
pain catastrophizing scale score
Time Frame: one time in one year
|
numerical value obtained using pain catastrophizing scale score
|
one time in one year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Beck depression inventory
Time Frame: one time in one year
|
numerical value obtained using Beck depression inventory
|
one time in one year
|
beck anxiety inventory
Time Frame: one time in one year
|
numerical value obtained using beck anxiety inventory
|
one time in one year
|
visual analog scale score
Time Frame: one time in one year
|
numerical value obtained using visual analog scale score
|
one time in one year
|
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 (Actual)
April 15, 2016
Primary Completion (Actual)
April 15, 2017
Study Completion (Actual)
April 15, 2017
Study Registration Dates
First Submitted
March 30, 2016
First Submitted That Met QC Criteria
April 1, 2016
First Posted (Estimate)
April 4, 2016
Study Record Updates
Last Update Posted (Actual)
June 19, 2018
Last Update Submitted That Met QC Criteria
June 16, 2018
Last Verified
June 1, 2018
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 16-KAEK-071
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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