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Sodium Bicarbonate for the prevention of contrast induced nephropathy in patients suspected with acute pulmonary embolism undergoing CTPA.

Sodium Bicarbonate for the prevention of contrast induced nephropathy in patients suspected with acute pulmonary embolism undergoing CTPA.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON25804
Enrollment
264
Registered
2009-08-18
Start date
2009-07-09
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Contrast Induced Nephropathy (contrastnefropathie) CT-pulmonary angiography (CTPA) Sodium bicarbonate (natriumbicarbonaat) Prevention (preventie)

Interventions

1. Sodium Bicarbonate 1 hour prior to CTPA 1 ml/kg bodyweight
2. CTPA without any hydration.

Sponsors

Name: Judith Kooiman Address: Leiden University Medical Center, Albinusdreef 2, Postzone C4-70, 2333 ZA Leiden, The Netherlands email: j.kooiman@lumc.nl tel: +31 (0)71-526.20.85
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Clinical suspected PE with an indication for CT-PA with intravenous administration of iso-osmolair contrast media and eGFR < 60 ml/min.

Exclusion criteria

Exclusion criteria: 1. Age < 18 years; 2. Exposure to contrast media within 7 days; 3. Pregnancy; 4. Allergy to contrastmedia; 5. Systolic bloodpressure < 100 mmHg.

Design outcomes

Primary

MeasureTime frame
Mean increase in serumcreatinine 2-4 days after CT-PA.

Secondary

MeasureTime frame
1. Increase in serum creatinine > 25% or > 44 umol/l, 3 days (+/- 1 day) after CT-PA with contrast media; 2. Increase in serum creatinine >25% or > 44 umol/l 2 months after CTPA with contrast media or the need for dialysis; 3. Increase in C-cystatine and NGAL 3 days (+/- 1 day) after CT-PA; 4. Increase in NGAL 2 hours after CT-PA.

Contacts

Public ContactJudith Kooiman

Leiden University Medical Center, Albinusdreef 2, Postzone C4-70

j.kooiman@lumc.nl+31 (0)71-526.20.85

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)