Evaluation of the depth of sedation under different methods of propofol during drug induced sleep endoscopy

Evaluation of the depth of sedation under different methods of propofol during drug induced sleep endoscopy - PROMISE

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00028603

Enrollment

100

Registered

2022-03-29

Start date

2020-01-13

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

G47.3 R06.5

Interventions

Group 1: Propfol 16mg/kg/h Group 2: Propfol 18mg/kg/h Group 3: Propfol 20mg/kg/h Group 4: Propfol 22mg/kg/h Group 5: Propfol 24mg/kg/h Group 6: Propofol Bolus 10mg BIS adopted

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Snoring and obstructive sleep apnea

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

Measure	Time frame
Depth of sedation (BIS)	—

Secondary

Measure	Time frame
Course of the sedation	—

Countries

Germany

Contacts

Public ContactMichael Herzog

Carl-Thiem-Klinikum

m.herzog@ctk.de+49355462849

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026