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NCT06341933
Risk Factors for AKI in Patients Undergoing VATS for Pulmonary Resection
trial testing Duration of Surgery in Acute Kidney Injury in 100 participants. Currently enrolling.
15 July 2025
Quick facts
| Lead sponsor | Atatürk Chest Diseases and Chest Surgery Training and Research Hospital |
|---|---|
| Status | Recruiting now |
| Study type | OBSERVATIONAL |
| Enrollment | 100 |
| Start date | 15 April 2024 |
| Primary completion | 15 July 2025 |
| Estimated completion | 15 December 2025 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Duration of Surgery
- Volume of Fluid in Surgery
- Blood Loss
Conditions studied
- Acute Kidney Injury — all drugs for Acute Kidney Injury →
- Surgery — all drugs for Surgery →
- Lung Cancer — all drugs for Lung Cancer →
Sponsor
Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
Who can join
Adults 18 to 65, any sex, with Acute Kidney Injury or Surgery. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study aims to investigate the potential factors contributing to the development of Acute Kidney Injury (AKI) in patients undergoing pulmonary resection with Video Assisted Thoracoscopic Surgery (VATS) for lung malignancy. The study will focus on demographic data, laboratory parameters, perioperative fluid management, and haemodynamics. The research will be conducted at SBÜ Ankara Atatürk Sanatorium Training and Research Hospital. The study will involve patients who have given informed consent and will undergo VATS with standard anaesthesia monitoring. Anaesthesia management will follow our routine protocol in our clinic. Patients will be divided into two groups based on whether they have a more than 25% decrease in estimated glomerular filtration rate (t-GFH) and/or a 1.5-fold increase in serum creatinine and/or a 6-hour urine volume of less than 0.5 ml/kg/h. The patients will be divided into two groups based on this definition, and the risk factors between these groups will be analysed. The preoperative routine blood values, demographic data (age, gender, height, weight, and BMI), ASA physical status, smoking and alcohol habits, comorbidities, and regular medication use will be recorded. Intraoperative urine output and haemodynamic parameters will also be monitored. Routine blood gas analysis, blood urea nitrogen (BUN), glomerular filtration rate (GFR), albumin, haemoglobin, sodium, potassium, chlorine, and magnesium will be measured and recorded, along with urine output and t-GFH. Patients will be evaluated in the hospital on the day the surgeon calls for a postoperative check-up and on the 30th postoperative day to see if there are any complications.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06341933
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT06341933 (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 Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
- Last refreshed: 30 January 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/NCT06341933.
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