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Recruiting NCT06341933

NCT06341933 Risk Factors for AKI in Patients Undergoing VATS for Pulmonary Resection

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Clinical Trial Summary
NCT ID NCT06341933
Status Recruiting
Phase
Sponsor Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
Condition Acute Kidney Injury
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2024-04-15
Primary Completion 2025-07-15

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 65 Years
Study Type OBSERVATIONAL
Interventions
Duration of SurgeryVolume of Fluid in SurgeryBlood Loss

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 100 participants in total. It began in 2024-04-15 with a primary completion date of 2025-07-15.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * Over 18 years of age, under 65 years of age, * American Society of Anesthesiologists (ASA) physical status 1-3, * Data of patients who will undergo wedge resection, segmentectomy or lobectomy with elective VATS due to lung malignancy will be examined prospectively. Exclusion Criteria: * Patients with a body mass index (BMI) less than 18.5kg/m2 or greater than 35 kg/m2, * Those with impaired renal function (the upper limit of the creatinine reference range is more than 50%; 1.3 mg/dL for men and 1.1 mg/dL for women), * A radiological examination was performed using radiocontrast material in the preoperative period, * Clinically and radiologically diagnosed with congestive heart failure and treatment has been started, * Having a history of pulmonary edema, * Those who have used steroids and non-steroidal anti-inflammatory drugs for a long time (exceeding 30 days), * Intubated to intensive care unit, * In need of massive peroperative blood transfusion, * Patients with deficiencies in the parameters examined will be excluded from the study.

Contact & Investigator

Central Contact

Ali ALAGÖZ, professor

✉ mdalagoz@gmail.com

📞 5079193765

Principal Investigator

Ali ALAGÖZ, professor

PRINCIPAL INVESTIGATOR

Ankara Ataturk Sanatorium Training and Research Hospital

Frequently Asked Questions

Who can join the NCT06341933 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Acute Kidney Injury. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06341933 currently recruiting?

Yes, NCT06341933 is actively recruiting participants. Contact the research team at mdalagoz@gmail.com for enrollment information.

Where is the NCT06341933 trial being conducted?

This trial is being conducted at Ankara, Turkey (Türkiye).

Who is sponsoring the NCT06341933 clinical trial?

NCT06341933 is sponsored by Atatürk Chest Diseases and Chest Surgery Training and Research Hospital. The principal investigator is Ali ALAGÖZ, professor at Ankara Ataturk Sanatorium Training and Research Hospital. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology