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

• Status: Unknown status
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

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.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Rikshospitalet University Hospital
• Treatments: Atropine

Criteria

Inclusion Criteria:

• Patients in ASA-group 1-2

• Operations (anal fissures, anal fistulas and haemorrhoids) lasting for less than one hour

• informed consent

• BMI <30

Exclusion Criteria:

• Patients using any medication known to influence the autonomous nervous system

• Patients with contraindications to atropine (e.i. fibrillation, glaucoma ect)

• BMI >30

• Pregnancy