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

Conditions

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

Tokat Gaziosmanpasa University

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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