Skip to main content
Clinical Trials/NCT00327938
NCT00327938
Completed
Not Applicable

Genetically Variation - May the Need of Opioids During Surgery be Known Beforehand by Giving Noxious Stimulation and Measure the Skin Conductance Response Before Surgery?

Rikshospitalet University Hospital1 site in 1 country50 target enrollmentMay 2006
ConditionsPain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
Rikshospitalet University Hospital
Enrollment
50
Locations
1
Primary Endpoint
skin conductance response
Status
Completed
Last Updated
19 years ago

Overview

Brief Summary

The purpose of this study is to find out if the tetanic noxious stimuli and the measured skin conductance response can be used as a test in patients before surgery to have an indication about what amount of analgesics the patient will need during surgery.

Detailed Description

Skin Conductance (SC) shows the emotional state as reflected in changes in the sympathetic nervous system. During sleep or other states of low basic sympathetic activity, activation of the sympathetic nervous system results in filling of the palmar and plantar sweat glands, and the SC increases transiently before the sweat is removed and the SC decreases again. When a short lasting outgoing sympathetic nervous burst occurs, fluctuations of SC will follow. An increase in the number of SC fluctuations (NSCF) can therefore be interpreted as increased activity in this part of the sympathetic nervous system. When remifentanil, an opioid analgetic is given, NSCF is reduced. Genetic variation influences the pharmacokinetics and the pharmacodynamics of analgesics like morphine derivates and remifentanil. 50 female patients will therefore be blood tested to study if they are Val/Val or Met/Met for the COMT gene, or if they are homozygous or heterozygous for the 118G allele and the 118A allele. This study will show if skin conductance can be used to measure noxious stimulation response before surgery (by giving a tetanic stimuli), and then predict what level of analgesic a patient will need during surgery.

Registry
clinicaltrials.gov
Start Date
May 2006
End Date
TBD
Last Updated
19 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
Rikshospitalet University Hospital

Eligibility Criteria

Inclusion Criteria

  • Women in American Society of Anesthesiologists (ASA) group 1-2 and with body mass index between 20 and 30 and going through laparoscopic surgery at the Gynecological Department, Ullevål University Hospital.
  • Normal renal and hepar function (serum albumin and serum creatinine should be within the normal limit).

Exclusion Criteria

  • Chronic pain in the last 6 months or recent use and abuse of analgesics.

Outcomes

Primary Outcomes

skin conductance response

Study Sites (1)

Loading locations...

Similar Trials