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Clinical Trials/NCT00374504
NCT00374504
Completed
Not Applicable

Prediction of Postoperative Pain by an Electrical Pain Stimulus

Rigshospitalet, Denmark1 site in 1 country46 target enrollmentSeptember 11, 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cesarean Section
Sponsor
Rigshospitalet, Denmark
Enrollment
46
Locations
1
Status
Completed
Last Updated
19 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
September 11, 2006
End Date
TBD
Last Updated
19 years ago
Study Type
Observational
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Healthy pregnant women scheduled for elective cesarean section

Exclusion Criteria

  • ASA III -IV
  • Chronic pain conditions.
  • Pacemaker.

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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