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Prediction of Post-Cesarean Section Pain

NCT00799162 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 800

Last updated 2011-09-26

No results posted yet for this study

Summary

The purpose of this study is to determine if dynamic psychophysical testing along with genetic screening will allow to identify pre-operatively women who will suffer severe acute pain post-operatively and the subset who may experience chronic pain following cesarean section.

Conditions

  • Postoperative Pain

Interventions

OTHER

Psychophysical testing, questionnaires, and genetics

pre-operative psychophysical testing of endogenous pain modulation, pre-operative questionnaires, peri- and post-operative data collection, long term follow-up assessing chronic pain, SNP association analysis, and whole genome scanning association studies

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-11-30
Primary Completion
2012-11-30
Completion
2013-11-30

Countries

  • United States
  • Belgium
  • Brazil
  • Singapore

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00799162 on ClinicalTrials.gov