Prediction of Postoperative Pain by an Electrical Pain Stimulus
NCT ID: NCT00374504
Last Updated: 2006-09-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
46 participants
OBSERVATIONAL
Brief Summary
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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.
Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Chronic pain conditions.
* Pacemaker.
18 Years
FEMALE
No
Sponsors
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Rigshospitalet, Denmark
OTHER
Principal Investigators
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Per Rotbøll Nielsen, MD
Role: PRINCIPAL_INVESTIGATOR
Rigshospitalet, Denmark
Locations
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Copenhagen University Hospital, Rrigshospitalet
Copenhagen, , Denmark
Countries
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References
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Nielsen PR, Norgaard L, Rasmussen LS, Kehlet H. Prediction of post-operative pain by an electrical pain stimulus. Acta Anaesthesiol Scand. 2007 May;51(5):582-6. doi: 10.1111/j.1399-6576.2007.01271.x.
Other Identifiers
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01 2745584
Identifier Type: -
Identifier Source: org_study_id