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The prednisolone prescription effect on post CABG surgery inflammatory mediators

Comparing the effect of continuous infusion of low dose Methyl Prednisolone with its single dose on reducing the inflammatory mediators and improvement of renal function in patients who undergo open heart surgery

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201010022622N2
Enrollment
100
Registered
2011-03-05
Start date
2010-11-11
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

coronary artery disease. Ischaemic heart diseases

Interventions

Intervention 1: In control group 15mg/Kg Prednisolone bolus dose before operation and after sedation will be prescribed. After operation this group will be had steady infusion of normal saline (2mg/Kg
Placebo
Treatment - Drugs
In control group 15mg/Kg Prednisolone bolus dose before operation and after sedation will be prescribed. After operation this group will be had steady infusion of normal saline (2mg/Kg/d)
Intervention group will be prescribed 1mg/Kg dose of prednisolone (bolous dose) before operation and 2mg/Kg/d as infusion after that.

Sponsors

Tehran Heart Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:1- age over 18. 2- written informed consent. 3- patients who are candidate for open heart surgery. Exclusion criteria: 1- recent use of systemic corticosteroid. 2- history of bacterial or fungal infection in the past two weeks. 3- history of sensitivity to corticosteroids. 4- uncontrolled diabetes mellitus. 5- history of renal failure 6- liver failure or elevated liver enzymes.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Length of stay in ICU and Intubation time. Timepoint: after transferring the patient to surgery ward. Method of measurement: questionnaire.

Secondary

MeasureTime frame
Reduction of inflammatory mediators. Timepoint: before, 6 and 48 hours following operation. Method of measurement: Blood test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Khosrow Barkhordari

Tehran Heart Center

Kbarkhordari@sina.tums.ac.ir+98 21 8802 9600

Outcome results

None listed

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