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Clinical Trials/DRKS00009002
DRKS00009002
Completed
未知

Influence of intraoperative opioids on quantitative sensory testing.

niversitätsklinikum Schleswig-Holstein,Campus Kiel,Klinik für Anästhesiologie und Operative Intensivmedizin0 sites23 target enrollmentAugust 28, 2015
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Conditionsopioid induced hyperalgesia (OIH)R20.8Other and unspecified disturbances of skin sensation

Overview

Phase
未知
Intervention
Not specified
Conditions
opioid induced hyperalgesia (OIH)
Sponsor
niversitätsklinikum Schleswig-Holstein,Campus Kiel,Klinik für Anästhesiologie und Operative Intensivmedizin
Enrollment
23
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 28, 2015
End Date
March 31, 2011
Last Updated
last year
Study Type
Interventional
Sex
Female

Investigators

Sponsor
niversitätsklinikum Schleswig-Holstein,Campus Kiel,Klinik für Anästhesiologie und Operative Intensivmedizin

Eligibility Criteria

Inclusion Criteria

  • •Age \>18 years
  • •ASA physical status I\-III
  • •elective surgery of the female breast, including segmental resections or mastectomy with or without sentinel lymph node biopsy
  • •written informed consent

Exclusion Criteria

  • •allergies to remifentanil, sufentanil or paracetamol, preoperative acute or chronic pain states, preoperative intake of any analgesic drugs, history of drug or alcohol abuse, renal insufficiency (serum creatinin \>1,5 mg/dl), impaired liver function (GTT \>100U/l), neurologic diseases that might have an impact on QST (PNP, ED), gravidity, diabetes mellitus

Outcomes

Primary Outcomes

Not specified

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