Evaluation of using Richmond score on patients admitted to intensive care unit

Evaluation of the use of the Richmond tool in opioid need and its effects on the hemodynamic status of patients admitted to intensive care unit after coronary artery bypass grafting

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190325043107N23

Enrollment

Registered

2021-03-27

Start date

2021-04-04

Completion date

Unknown

Last updated

2021-04-26

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

Conditions

Sedation. Failed moderate sedation during procedure

Interventions

Intervention 1: Intervention group: Patients will be included in this group after random allocation. In this study, patients are connected to a ventilator and will be evaluated according to the criter

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Candidate for coronary artery bypass graft surgery Fractional ejection between 35 and 40

Exclusion criteria

Exclusion criteria: Urgency of surgery Heart failure Opioid addiction

Design outcomes

Primary

Measure	Time frame
Sedation. Timepoint: Every six hours for three days. Method of measurement: Richmond Relaxation Score.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi Khanbabayi Gol

Tabriz University of Medical Sciences

Khanbabayimehdi69@gmail.com+98 41 3334 7054

Outcome results

None listed

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