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OpenTrials
Completed

NCT Number: NCT07020130

Risk Factors,PREvention and OutComes for CI-AKI in PatientS undErgoing PCI (PRECISE)

A prospective observational study included all patients undergoing percutaneous coronary intervention(PCI) in Fujian Provincial Hospital from January 1st 2012 to December 31st 2018. The aim was to determine the incidence,risk factors,prophylactic strategy and outcomes of CI-AKI in patients undergoing PCI.

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Key information

Conditions

CIN

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Fuzhou, Fujian, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Critically ill patients undergoing PCI at ICU

Exclusion criteria

  • pregnancy lactation end-stage renal disease (eGFR <15 mL/min/1.73 m2) long-term dialysis treatment intravascular administration of contrast medium within the last 7 or 3 days postoperatively

Treatment and study plan

Primary outcomes

  1. CI-AKI

    Time frame: 5 year

    This was due to acute kidney injury following the use of intravascular contrast media. Serum creatinine is the primary measuring modalities.

  2. CKD

    Time frame: 5 year

    Chronic renal structural and functional disorders that occurred during follow-up after administration of intravascular contrast agents, estimated glomerular filtration rate (eGFR) as the primary measuring modalities.

Secondary outcomes

  1. all-cause mortality

    Time frame: 5 year

    Defined as deaths occurring during follow-up after discharge from EPCI, excluding force majeure factors such as natural disasters and car accidents,and the necessary information was gathered during follow-up.

Sponsors and collaborators

Lead sponsor

Kaiyang Lin

Other

Registry information

Official study title

Risk Factors,PREvention and outComes for Contrast-Induced Acute Kidney Injury in patientS undErgoing Percutaneous Coronary Intervention:a Single-center Cohort Study(PRECISE)

Acronym: PRECISE

Important dates

Study start
2012
Primary completion
2018
Study completion
2018
First posted
Jun 13, 2025
Registry last updated
Jun 13, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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