Prediction of Postoperative Pain by an Electrical Pain Stimulus
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|ClinicalTrials.gov Identifier: NCT00374504|
Recruitment Status : Completed
First Posted : September 11, 2006
Last Update Posted : September 11, 2006
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.
|Condition or disease|
|Study Type :||Observational|
|Estimated Enrollment :||46 participants|
|Observational Model:||Case Control|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00374504
|Copenhagen University Hospital, Rrigshospitalet|
|Copenhagen, Denmark, dk-2100|
|Principal Investigator:||Per Rotbøll Nielsen, MD||Rigshospitalet, Denmark|