Prediction of Postoperative Pain by an Electrical Pain Stimulus

Status Completed

Clinical Trial Summary

The aim of this study is to evaluate a possible correlation between predictive precesarean section pain and development of postcaesarean section pain using the PM.

Patients and Methods 46 healthy pregnant women scheduled for elective cesarean section is included after informed consent. The standard operation procedures included spinal anesthesia, paracetamol 1 g 8 hourly, diclofenac 50 mg 8 hourly and oxycontine 10 mg x 2. Morphine was used for break-through pain.

Before cesarian section the threshold for sensory and pain were measured 3 times, and the average was used for analyses. After cesarian section a blinded midwife assess the pain at rest and during mobilization every 12th hours over 2 days score.

Data was analyzed using AUC and non-parametric test, P < 0,05.

Clinical Trial Description

n/a

Study Design

Observational Model: Case Control, Time Perspective: Longitudinal

Related Conditions & MeSH terms

Cesarean Section

Clinical Trial Details

NCT number	NCT00374504
Study type	Observational
Source	Rigshospitalet, Denmark
Contact
Status	Completed
Phase	N/A

View Details

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