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Does N-Acetylcysteine (Parvolex®) prophylaxis reduce the incidence of renal impairment after onpump Coronary Artery Bypass Graft surgery? A prospective randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN71629284
Enrollment
224
Registered
2007-08-21
Start date
2007-08-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Renal impairment Urological and Genital Diseases Renal diseases

Interventions

For both groups, there will be no change in routine anaesthetic/surgical or post operative management. The intervention group will be administered 2 g N-Acetylcysteine on the night before surgery (or

Sponsors

University Hospital of South Manchester NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective coronoray artery bypass surgery (onpump) at Wythenshawe Hospital 2. Aged 21 - 80 years

Exclusion criteria

Exclusion criteria: 1. Urgent or emergency cases 2. History of hypersensitivity to N-Acetylcysteine 3. Patients already taking N-Acetylcysteine 4. Patients with renal failure

Design outcomes

Primary

MeasureTime frame
Creatinine clearance and serum creatinine levels on second and fifth post operative day and on discharge.

Secondary

MeasureTime frame
Length of Intensive Care Unit (ICU) stay.

Countries

United Kingdom

Outcome results

None listed

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