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Effects of N-acetyl cysteine on the improvement of cardiopulmonary and renal functions

Effects of N-acetyl cysteine on the improvement of cardiopulmonary and renal functions after cardiopulmonary bypass in patients with coronary artery bypass graft

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150825023760N8
Enrollment
50
Registered
2019-03-12
Start date
2013-12-10
Completion date
Unknown
Last updated
2019-03-25

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

Conditions

Cardiac coronary arterial disease. I26-I28

Interventions

Intervention 1: Intervention group: After induction, a central venous line was inserted and first blood sample (pre-CPB time) was obtained. After this stage, the NAC group received 100 mg/kg NAC. Int

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria were patients with age 25-75 years undergoing cardio pulmonary bypass (CPB) for coronary artery bypass graft(CABG).

Exclusion criteria

Exclusion criteria: Exclusion criteria were patients for emergency coronary artery bypass graft(CABG) Redo CABG The intubation time after surgery for more than >10 hours Severe hemorrhage during coronary artery bypass graft (CABG)

Design outcomes

Primary

MeasureTime frame
Interleukin-6. Timepoint: The time points of blood sampling were after induction, before the administration of N-acetylcysteine (NAC) (pre-CPB)(Time 1) as baseline, one hour after CPB (on-CPB)(Time 2) , and one hour after that the patients were off-CPB (post-CPB)(Time 3). Method of measurement: Interleukin-6 measurement kit was used to measure Interleukin-6.;Shunt. Timepoint: The time points of blood sampling were after induction, before the administration of N-acetylcysteine (NAC) (pre-CPB)(Time 1) as baseline, one hour after CPB (on-CPB)(Time 2) , and one hour after that the patients were off-CPB (post-CPB)(Time 3). Method of measurement: Using the formula used to measure it.;Compliance reactive protein (CRP). Timepoint: The time points of blood sampling were after induction, before the administration of N-acetylcysteine (NAC) (pre-CPB)(Time 1) as baseline, one hour after CPB (on-CPB)(Time 2) , and one hour after that the patients were off-CPB (post-CPB)(Time 3). Method of measurement: Compliance reactive protein (CRP) measurement kit was used to measure Compliance reactive protein (CRP).;CKMB. Timepoint: The time points of blood sampling were after induction, before the administration of N-acetylcysteine (NAC) (pre-CPB)(Time 1) as baseline, one hour after CPB (on-CPB)(Time 2) , and one hour after that the patients were off-CPB (post-CPB)(Time 3). Method of measurement: Creatine kinase-muscle/brain (CKMB) measurement kit was used to measure creatine kinase-muscle/brain (CKMB).;Troponine. Timepoint: The time points of blood sampling were after induction, before the administration of N-acetylcysteine (NAC) (pre-CPB)(Time 1) as baseline, one hour after CPB (on-CPB)(Time 2) , and one hour after that the patients were off-CPB (post-CPB)(Time 3). Method of measurement: Troponine measurement kit was used to measure Troponine.;Serum Lactate. Timepoint: The time points of blood sampling were after induction, before the administration of N-acetylcysteine (NAC)

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadreza Jamshidi

Zanjan University of Medical Sciences

jamshidianes@zums.ac.ir+98 24 3313 0000

Outcome results

None listed

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