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Prediction of Postoperative Pain by an Electrical Pain Stimulus

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Rigshospitalet

Status

Completed

Conditions

Cesarean Section

Study type

Observational

Funder types

Other

Identifiers

NCT00374504
01 2745584

Details and patient eligibility

About

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.

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Healthy pregnant women scheduled for elective cesarean section

Exclusion criteria

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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