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Does prophylactic N-AcetylCysteine decrease incidence of contrast nephropathy in patients undergoing peripheral angiography?

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN35882618
Enrollment
40
Registered
2007-08-02
Start date
2007-05-01
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

Contrast induced nephropathy Urological and Genital Diseases Nephropathy

Interventions

Treatment group: Patients will be given 600 mg twice daily N-acetylcysteine the day before the angiogram, and 600 mg twice on the day of the angiogram with intravenous fluids. Samples of urine and b

Sponsors

Cambridge University Hospital NHS Trust (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Any patient undergoing peripheral angiography in the Cambridge Vascular Unit, Addenbrooke?s Hospital, Cambridge who consents to participation.

Exclusion criteria

Exclusion criteria: 1. Any patient undergoing peripheral angiography in Cambridge Vascular Unit 2. Any patient that does not consent to participation in the study 3. Any patient under the age of 18 years 4. Any patient with established renal failure on renal replacement therapy (dialysis)

Design outcomes

Primary

MeasureTime frame
Primarily we are looking for a reduction in the elevation in Albumin/Creatinine ratio and also of other markers of renal damage in urine (retinol binding protein), using the samples collected before the angiogram and first, second and third day post angiography.

Secondary

MeasureTime frame
A reduction in the mortality and morbidity related to renal failure that may result secondary to contrast solution used in angiography; this 30-day mortality morbidity reduction will be measured on follow up in clinic normally four to six weeks post angiography.

Countries

United Kingdom

Outcome results

None listed

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