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Prediction of Post-Cesarean Section Pain

Prediction of Post-Cesarean Section Pain

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00799162
Acronym
PPCSP
Enrollment
800
Registered
2008-11-27
Start date
2008-11-30
Completion date
2013-11-30
Last updated
2011-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Brief 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.

Interventions

OTHERPsychophysical 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

University of Washington
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Women age 18-50 scheduled for an elective cesarean section (1st or 2nd cesarean section)

Exclusion criteria

Women who: * have taken opioids, acetaminophen, or NSAIDs 48 hrs prior to psychophysical testing * have had more than two previous cesarean sections * have a vertical abdominal incision from a prior cesarean section * are non-English speaking * have mental health issues * have a failure of spinal anesthetic and require conversion to general anesthesia * have a vertical uterine incision performed during ongoing cesarean section * have a previous vertical uterine scar discovered during ongoing cesarean section

Countries

Belgium, Brazil, Singapore, United States

Contacts

Primary ContactLisa Y Flint, BS
lyflint@u.washington.edu(206) 543-7817
Backup ContactKatrina L Golub, MPH
kgerber@u.washington.edu(206) 616-9209

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026