N/A
N=575
Persistent Pain After CS Delivery
Persistent Pain After Delivery
Bottom Line
View on ClinicalTrials.gov: NCT01996592 ↗Enrolled (actual)
575
Serious AEs
0.0%
Results posted
Aug 2018
Primary outcome: Primary: Persistent Pain-PERCEIVED STRESS Scores Stratified by the Rate of Recovery — 11.4; 12.9; 15.4 units on a scale — p=<0.01
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Adult · 18+ yrs
- Sex
- Female
- Sponsor
- Wake Forest University Health Sciences
- Primary completion
- Jan 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Persistent Pain-PERCEIVED STRESS Scores Stratified by the Rate of Recovery |
11.4; 12.9; 15.4 | <0.01 sig |
| PRIMARY Persistent Pain-EMOTIONAL DISTRESS |
10.7; 11.5; 12.8 | <0.01 sig |
Summary
Many factors influence the development of persistent pain after CS (chronic pain) as well as post-partum depression. We are attempting to use trajectory pain methods in an attempt to identify those at risk for the development of persistent pain post delivery using a daily method of contact for the determination of pain scores. Assessments are also done evaluating satisfaction of pain management and maternal/infant bonding opportunities. Physical activity is monitored by subject's wearing a Fitbit with correlation being done with pain scores obtained over 60 days postop with eligible subjects..
Eligibility Criteria
Inclusion Criteria
- >/= 18 years of age English speaking
Exclusion Criteria
non-English speaking
Data sourced from ClinicalTrials.gov (NCT01996592). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.