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Reduced incidence of nausea and vomiting (PONV) in sevoflurane anaesthesia due to low-dose propofol infusion

Reduced incidence of nausea and vomiting (PONV) in sevoflurane anaesthesia due to low-dose propofol infusion - PONV

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00008568
Enrollment
686
Registered
2015-06-01
Start date
2014-11-01
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

M16.1 K40.9

Interventions

Group 1: General anaesthesia will be performed by total intravenous anaesthesia (TIVA) using propofol and the opiate remifentanile in combination with measurement of depth of anaesthesia by electroenc

Sponsors

Park-Klinik WeissenseeAbteilung Anästhesiologie Intensivmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients undergoing elective surgery under general anaesthesia Endotracheal intubation Minimum age of 18 years ASA-classification I-III Minimum duration of operation 30 minutes Good knowledge of German for understanding

Exclusion criteria

Exclusion criteria: Lack of willingness to accept storage and transfer of pseudonymised health data Emergency surgery Pregnancy Inoperable regarding the ASA-classification Artificial ventilation postoperatively Lack of an informed consent Age under 18 years Participation in an other study during the last three month Mental disorders History of an adverse reaction to study medication

Design outcomes

Primary

MeasureTime frame
prevalence and severity of PONV (acquired by postoperative questionnaire, day of surgery, first and second postoperative day)

Secondary

MeasureTime frame
sevoflurane concentration( Vol%exp) at a given depth of anaesthesia (Narcotrend-signal: D2-E0) and a fix propofol dosage (1 µg/ml, TCI-modus) [intraoperative measurement] use of vasoactive substances such as norepinephrine [intraoperative measurement and recovery room] pain level and need in analgesics postoperatively [recovery room, day of surgery, first and second postoperative day] duration of stay in recovery room [postoperative measurement] cognitive function [1 day preoperatively, recovery room, first and second postoperative day]

Countries

Germany

Contacts

Public ContactMario Hensel

Park-Klinik WeissenseeAbteilung Anästhesiologie Intensivmedizin

hensel@park-klinik.com0049 30 9628 3502

Outcome results

None listed

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