FEASABILITY TEST OF A HANDSET DEVICE TO DETECT SEDATION LEVELS AND LOSS OF CONSCIOUSNESS DURING PROPOFAL ADMINISTRATION.

FEASABILITY TEST OF A HANDSET DEVICE TO DETECT SEDATION LEVELS AND LOSS OF CONSCIOUSNESS DURING PROPOFAL ADMINISTRATION. - Feasability test of a handset device

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON35328

Enrollment

Registered

2011-11-30

Start date

2011-12-01

Completion date

Unknown

Last updated

2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

heeft geen betrekking op een aandoening. Heeft te maken met het ontwikkelen van een nieuw medisch device loss of consciousness sedation levels

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Twenty patients requiring anesthesia for clinical surgical care ASA physical status I, II or III Age 50 - 72 years

Exclusion criteria

Exclusion criteria: Volunteer refusal Significant cardiovascular or respiratory disease latex allergy

Design outcomes

Primary

Measure	Time frame
Response times (button press in response to vibration of a hand set) will be recorded electronically (automatically) during induction of anesthesia in routine clinical care in order to detect level of sedation and loss of consciousness.	—

Secondary

Measure	Time frame
none	—

Countries

Netherlands

Outcome results