Perioperative Use of NAC to Prevent AKI in Patients With Pre-existing Moderate Renal Insufficiency Following Cardiac Surgery

Sponsor
Ain Shams University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05555511
Collaborator
(none)
46
1
2
6
7.6

Study Details

Study Description

Brief Summary

Acute kidney injury (AKI) or renal impairment is an established complication of cardiac surgery occurring with an incidence up to 30%, To date, no agent has conferred renal protection. Considerable interest has developed in the potential for Nacetylcysteine (NAC) to exert a renoprotective effect in patients undergoing cardiac surgery. Due to the beneficial effect of NAC on contrast nephropathy and its reported anti-inflammatory effects.

Condition or Disease Intervention/Treatment Phase
  • Other: Control Group
N/A

Detailed Description

Acute kidney injury (AKI), is a well-known complication of cardiac surgery, with an incidence of up to 30% depending on the definition. AKI caused by cardiac surgery is the second most common cause of AKI in the intensive care unit and is a common and serious postoperative complication of cardiac surgery requiring cardiopulmonary bypass (CPB).

The pathogenesis of AKI after CPB is multifactorial, and is mostly due to hypo perfusion, reperfusion injury, activation of the systemic inflammatory response, and/or low cardiac output. Reperfusion will result in the formation of reactive oxygen species, resulting in injury to tissues.

The activation of the systemic inflammatory response is mostly due to the exposure of blood to the extracorporeal CPB circuit, resulting in the activation of the immune system, which is also mediated by the generation of reactive oxygen species. This results in increased recruitment of neutrophils, macrophages, and lymphocytes into the renal parenchyma, leading to AKI.

N-acetylcysteine (NAC) is well known for its antioxidant and free-radical scavenging properties, as well as its vasodilator properties. Its antioxidant properties enable it to prevent ischemic cell death, and as a free-radical scavenger, NAC mitigates the effect of increased reactive oxygen species caused by reperfusion. Hence, theoretically, NAC is able to counteract several mechanisms of kidney injury during cardiac surgery, namely, the systemic inflammatory response, free-radical injury, and ischemia.

In this study, we aimed to investigate if the perioperative use of acetylcysteine will prevent kidney injury after cardiac surgery.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
46 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Patients will be randomized using computer generated random series into two groups according to the used drug into: Group A: N-acetylcysteine group (23 Patients) Patients will receive N-acetylcysteine 600 mg intravenous(IV) every 12 hours 24 hours before surgery and will be continued for 48 hours after surgery. Group B : Standard (control) group (23 Patients) Patients will not receive N-Acetylcysteine and will receive standard care according to our institutional protocol.Patients will be randomized using computer generated random series into two groups according to the used drug into:Group A: N-acetylcysteine group (23 Patients) Patients will receive N-acetylcysteine 600 mg intravenous(IV) every 12 hours 24 hours before surgery and will be continued for 48 hours after surgery. Group B : Standard (control) group (23 Patients) Patients will not receive N-Acetylcysteine and will receive standard care according to our institutional protocol.
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Perioperative Use of N-acetylcysteine to Prevent Acute Kidney Injury in Patients With Pre-existing Moderate Renal Insufficiency Following Cardiac Surgery
Actual Study Start Date :
Aug 26, 2022
Anticipated Primary Completion Date :
Jan 26, 2023
Anticipated Study Completion Date :
Feb 26, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: N-acetylcysteine group

(23 Patients) Patients will recieve N-acetylcysteine 600 mg intravenous(IV) every 12 hours 24 hours before surgery and will be continued for 48 hours after surgery

Other: Control Group
Patients will not receive N-Acetylcystiene and will receive standard care according to our institutional protocol

No Intervention: Standard group

Patients will not receive N-Acetylcysteine and will receive standard care according to our institutional protocol

Outcome Measures

Primary Outcome Measures

  1. Serum Creatinine rise [7days]

    Creatinine increase >25% or ≥ 0.5 mg/dl above baseline

Secondary Outcome Measures

  1. RRT [7 days]

    Need for Renal Replacement Therapy

  2. Length of ICU stay [3 days]

    Length of stay in the ICU in days

  3. Length of hospital stay [7 to 10 Days]

    Length of stay in hospital in days

  4. Mortality [30 days]

    Mortality rate

  5. Adverse effects [2 days]

    Occurrence of NAC adverse effects as (bronchospasm, urticaria, facial edema, nausea/vomiting).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

Inclusion Criteria

  • Scheduled for open heart Surgery with cardiopulmonary bypass (CPB) pump.

  • Pre-existing moderate renal insufficiency serum creatinine more than 1.5 mg/dL

Exclusion Criteria:
  • Patients on hemodialysis preoperatively

  • History of renal transplantation

  • IV contrast within 4 days prior to surgery

  • Urgent/emergent surgery

  • Preoperative hemodynamic instability (intra-aortic balloon pump support or vasoactive medications)

  • Planned off-pump surgery;

  • Planned deep-hypothermic-circulatory-arrest

  • known or suspected allergy to NAC

  • Patient Refusal.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cardiothoracic Academy, Ain Shams University Hospitals Cairo Egypt 11566

Sponsors and Collaborators

  • Ain Shams University

Investigators

  • Principal Investigator: Mohamed A. Alhadidy, Ain Shams University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Mohamed Alaaeldin Abdelmoneem Alhadidy, Principal Investigator, Ain Shams University
ClinicalTrials.gov Identifier:
NCT05555511
Other Study ID Numbers:
  • FMASU R 122/2022
First Posted:
Sep 27, 2022
Last Update Posted:
Dec 28, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Mohamed Alaaeldin Abdelmoneem Alhadidy, Principal Investigator, Ain Shams University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 28, 2022