comparing post cardiac surgery neurological side effects in interventional group for maintain regional cerebral O2 saturation more than 50% versus non interventional group

Clinical trial comparing post cardiac surgery neurological side effects in interventional group for maintain regional cerebral O2 saturation more than 50% versus non interventional group

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20161022030421N2

Enrollment

200

Registered

2018-03-02

Start date

2017-12-23

Completion date

Unknown

Last updated

2018-03-26

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

Conditions

neurological side effects after cardiac surgery.

Interventions

Intervention 1: Interventional group:A group that monitoring of Cerebral oximetry (rScO2) will be performed .interventions were performed to maintain rScO2 at, or above the baseline value, including i

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: patients who underwent a cardiac surgery with cardiopulmonary bypass pump (CPB pump).

Exclusion criteria

Exclusion criteria: Patients with history of psychological disorder patients who were taking psychiatric drugs

Design outcomes

Primary

Measure	Time frame
Neurological side effects. Timepoint: Up to 72 hours after surgery. Method of measurement: Interview and neurological examination.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Lak

Bagheiat-allah University of Medical Sciences

marziehlak@bmsu.ac.ir+98 212449013

Outcome results

None listed

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