Effect of combination of intravenous propofol and inhaled nitrous oxide: a randomized clinical trial

Effect of combination of intravenous propofol and inhaled nitrous oxide: a randomized clinical trial - Effect of combination of intravenous propofol and inhaled nitrous oxide

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000009728

Enrollment

Registered

2013-01-08

Start date

2011-06-21

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

healthy adult volunteers

Interventions

sedation with and intravenous propofol sedation with and intravenous propofol and inhaled nitrous oxide

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Healthy adult volunteers

Exclusion criteria

Exclusion criteria: A history of cardiovascular disease, hypertension, respiratory disease and dysautonomia were considered criteria for exclusion from the study.

Design outcomes

Primary

Measure	Time frame
Hemodynamics, heart rate variability, depth of sedation	—

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026