Overview

Measurement of Psychomotor Recovery After Anesthesia Using 4CRT

Status:
Completed
Trial end date:
2019-06-25
Target enrollment:
0
Participant gender:
Female
Summary
The aim of the investigation is to validate the SmartPhone-based 4-Reaction Choice Time Test (4CRT) as a measure for recovery of the psychomotor function in patients after general anesthesia. One hundred female patients, scheduled to ambulatory gynecological surgery in general anesthesia, will be randomized to the group with pharmacological anxiolytic premedication with midazolam (N=50) and to the group without midazolam (N=50). All patients will be monitored using 4CRT before and after standardized general anesthesia. The reaction time, measured with 4CRT is the primary outcome parameter of the investigation.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University Medicine Greifswald
Collaborator:
Department of Anesthesiology, Hospital Dresden-Friedrichstadt, Dresden, Germany
Treatments:
Midazolam
Criteria
Inclusion Criteria:

- Physical status I-III according to American Society of Anesthesiology

- ambulatory gynecologic surgery of 10-40 min

- patient is able to use VAS and to use SmartPhone-based 4CRT

- given informed consent

Exclusion Criteria:

- age < 18 or > 50 years

- patients who are not able to give their informed consent

- surgery lasts more than 40 min.

- history of psychopharmaceuticals or analgesics