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NCT02373696 Clinical Trial

Chronic Pain Dynamic Psychophysical Tests and Genetic Screening

Pain Clinical Trial

Official title:
Prediction of Chronic Pain in the Asian Population- Comprehensive Programme Encompassing Dynamic Psychophysical Tests and Genetic Screening to Determine and Prevent Persistent Post-caesarean Pain

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02373696
Other study ID # 2010/160/D
Secondary ID
Status Completed
Phase N/A
First received February 22, 2015
Last updated September 3, 2015
Start date April 2010
Est. completion date January 2015

Study information
Verified date September 2015
Source KK Women's and Children's Hospital
Contact n/a
Is FDA regulated No
Health authority Singapore: Institutional Review Board
Study type Observational

Clinical Trial Summary

Incidence and risk factors for persistent post surgical pain after Caesarean section are investigated. Demographic, psychophysical testing and genetic screening factors are performed in the perioperative period. Phone survey is performed to investigate the incidence of persistent post surgical pain after Caesarean section.

Description:

Persistent post surgical pain after Caesarean section may lead to functional limitation and pain during activities of daily living. Demographic factors, psychophysical factors (mechanical temporal summation, diffuse noxious inhibitory control, state trait anxiety inventory) and genetic screening are used to predict the association with persistent post surgical pain. Phone survey follow up is performed to investigate the incidence of persistent post surgical pain and functional limitations due to pain experienced.

Recruitment information / eligibility
Status Completed
Enrollment 178
Est. completion date January 2015
Est. primary completion date January 2015
Accepts healthy volunteers No
Gender Female
Age group 21 Years to 50 Years
Eligibility Inclusion Criteria:

- Women undergoing spinal anaesthesia for Caesarean section

Exclusion Criteria:

- Failed spinal anaesthesia, Unable to perform psychophysical testing.

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Singapore KK Women's and Children's Hospital Singapore

Sponsors (1)
Lead Sponsor Collaborator
KK Women's and Children's Hospital

Country where clinical trial is conducted

Singapore, 

Outcome
Type Measure Description Time frame Safety issue
Primary Persistent Postsurgical Pain Pain experienced in the lower abdominal region and surgical area after Caesarean section 12 weeks No
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