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Measurement of Stress During Anesthesia With "Pain Detector" on Patients Receiving Atropine

NCT00328900 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2012-06-01

No results posted yet for this study

Summary

24 patients randomly divided into two groups, one of the groups receiving atropine in addition to the planned anaesthesia. Skin conductance parameters to be compared between the two groups.

Conditions

Interventions

DRUG

Administration of 0,7 mg of atropine

DEVICE

Measurement of skin conductance with Pain detector

Sponsors & Collaborators

  • Rikshospitalet University Hospital

    lead OTHER

Principal Investigators

  • Hanne Storm, PhD · Rikshospitalet University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-01-31

Countries

  • Norway

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00328900 on ClinicalTrials.gov