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NCT06889272
Investigation of the Relationship Between Blood Transfusion Volume and Development of Renal Failure in Pediatric Patients Undergoing Cardiovascular Surgery
trial testing blood transfusion in Congenital Cardiac Defect in 205 participants. Completed in 30 June 2024.
1 April 2024
Quick facts
| Lead sponsor | Hacettepe University |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 205 |
| Start date | 31 January 2024 |
| Primary completion | 1 April 2024 |
| Estimated completion | 30 June 2024 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- blood transfusion — full drug profile →
Conditions studied
- Congenital Cardiac Defect — all drugs for Congenital Cardiac Defect →
- Acute Renal Injury — all drugs for Acute Renal Injury →
- Blood Transfusion Complication — all drugs for Blood Transfusion Complication →
Sponsor
Hacettepe University
Who can join
Under 18, any sex, with Congenital Cardiac Defect or Acute Renal Injury. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Blood transfusion strategies in cardiac surgery are a research topic that has been studied more for adults. There is not enough data on this subject for children in studies. Investigators aim to examine the renal damage risk level of blood transfusion volume, which is one of the modifiable risk factors that can cause acute kidney injury in pediatric cases undergoing cardiac surgery. The main question it aims to answer is: What is the effect of blood transfusion volume on the risk of renal damage in pediatric cardiovascular surgery? The names of the patients who were operated on by the Department of Cardiovascular Surgery will be accessed from the system records and their files will be reviewed. The patients' demographic information, anesthesia management and postoperative renal function tests will be scanned.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
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Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06889272 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Hacettepe University
- Last refreshed: 21 March 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06889272.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing