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Comparisons between 5-Hour Preprocedural hydration vs 20-Hour Preprocedural hydration on Serum Creatinine in Patients with Renal Insufficiency Undergoing an Elective Coronary Procedure

Comparisons between 5-Hour Preprocedural hydration vs 20-Hour Preprocedural hydration on Serum Creatinine in Patients with Renal Insufficiency Undergoing an Elective Coronary Procedure - Comparisons between 5-Hour Preprocedural hydration vs 20-Hour Preprocedural hydration on Serum Creatinine in Patients with Renal Insufficiency Undergoing an Elective Coronary Procedure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005557
Enrollment
120
Registered
2011-05-06
Start date
2010-05-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

chronic kidney disease

Interventions

5h-HS (intravenous hydration with isotonic saline for 5 hours before contrast exposure and for 24 hours after contrast exposure) 20h-HS (intravenous hydration with isotonic saline for 20 hours befor

Sponsors

Oita Nakamura Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria were as follows: age of 20 - 85 years; estimated glomerular filtration rate (eGFR) of 15-60 L/min/1.73 m2.

Exclusion criteria

Exclusion criteria: Exclusion criteria were as follows: emergency coronary arteriography or percutaneous coronary intervention, allergy to contrast mediums, pregnancy, intravascular administration of contrast mediums within the preceding 5 days of the study, acute coronary syndrome within the preceding 1 month of the study, severe symptoms of heart failure (New York Heart Association functional class IV), left ventricular ejection fraction <25%, severe hepatic insufficiency, severe chronic respiratory disease, single function kidney, dialysis, and administration of N-acetylcysteine, theophylline, dopamine, or mannitol.

Design outcomes

Primary

MeasureTime frame
The primary endpoint was the absolute and % maximal changes in serum creatinine from the baseline up to 48 hours after contrast exposure.

Secondary

MeasureTime frame
The secondary endpoints were the incidence of CIN defined as a ≥25% increase in serum creatinine within 48 hours.

Countries

Japan

Contacts

Public Contactkumie torigoe

Oita Nakamura Hospital Division of Cardiovascular Medicine

kumiet@oita-u.ac.jp097-536-5050

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026