Comparison of the characteristics of patients treated with and without Propofol

Comparison of the characteristics of patients treated with and without Propofol in the intensive care unit of MasihDaneshvari Hospital.

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20150107020592N19

Enrollment

500

Registered

2018-07-29

Start date

2018-01-10

Completion date

Unknown

Last updated

2018-09-11

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

Conditions

Patients treated with and without Propofol in the intensive care unit..

Interventions

Intervention 1: Intervention group: treated with Propofol 10%. The drug that is used as a short intravenous injection method and it reduces the level of consciousness or anesthesia. For adult patients

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients need a sedative in the intensive care unit

Exclusion criteria

Exclusion criteria: Patients with propofol sensivity Patients with certain underlying conditions

Design outcomes

Secondary

Measure	Time frame
Blood pressure. Timepoint: Before and after the intervention. Method of measurement: Barometer.;Cardiac Output. Timepoint: Before and after intervention. Method of measurement: monitoring.	—

Primary

Measure	Time frame
Evaluate the effects and risks of using propofol. Timepoint: After using propofol. Method of measurement: The checklist includes demographic features and variables such as cardiac output, hypotension, hyperlipidemia, and sepsis.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyyed Mohammad Reza Hashemian

The Edjucational , Research and Treatment center

iran.criticalcare@yahoo.com+98 21 2610 9512

Outcome results

None listed

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