- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06000098
Consol Time and Acute Kidney Injury in Robotic-assisted Prostatectomy
Effect of Console Time on the Development of Acute Kidney Injury in Robotic-assisted Laparoscopic Prostatectomy
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Although open surgery has been used for a long time in the treatment of prostate diseases, robotic-assisted laparoscopic prostatectomy (RALP) has become more common in the last 20 years. The excellence in results has made the use of the robot the gold standard in prostate surgery. However, the presence of two critical factors during RALP surgery still bothers clinicians. The first of these is severe fluid restriction and the other is the deep Trendelenburg position and pneumoperitoneum. The prolongation of the robotic console time also causes the prolongation of fluid restriction and Trendelenburg time. This combination may cause significant pathophysiological changes in both the renal and cardiac systems and may lead to postoperative acute renal injury (AKI). AKI is a serious clinical complication with increasing incidence and is associated with adverse short-term and long-term outcomes worldwide, resulting in a large healthcare burden. Intraoperative advanced monitoring techniques can contribute to the prevention of renal damage that may occur by providing early recognition of these pathophysiological changes occurring in the renal and cardiac systems.
The aim of our study was to determine the effect of console duration on the incidence of AKI after RALP which was managed using intraoperative advanced monitoring techniques (pressure recording analytical method-PRAM). In addition, this study aimed to evaluate the ability of changes in hemodynamic parameters to predict the development of AKI in RALP patients who underwent restrictive fluid therapy.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Istanbul, Turkey, 31190
- Acibadem Altunizade Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients with American Society Of Anesthesiology physical status 1-3
- Underwent Robotic-assisted laparoscopic prostatectomy
- Underwent restrictive fluid therapy during the console period
Exclusion Criteria:
- Under 18 years of age
- Arrhythmia (atrial fibrillation, frequent premature beat)
- History of myocardial infarction in the last 3 months
- Heart failure
- Severe pre-existing lung disease
- Severe valvular heart disease
- Chronic renal disease on dialysis,
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Patients undergoing robotic-assisted laparoscopic prostatectomy in deep Trendelenburg position.
Patients with ASA( American Society of Anesthesiologists) physical status 1-3 who underwent robotic-assisted laparoscopic prostatectomy in deep Trendelenburg position with restrictive fluid therapy
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0,5 ml/hour fluid administration during prostatic anastomosis. After general anesthesia induction, the patients were placed in the deep Trendelenburg position (at least 25°-45° upside down).
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Console time was measured for evaluating the effect of restrictive fluid therapy and prostatic urethra anastomosis time on the development of acute kidney injury.
Time Frame: The duration of the measurement was defined as during the surgery.
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Console time ( minute) indicates the restrictive fluid therapy time, prostatic resection, and prostatic urethra anastomosis time.
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The duration of the measurement was defined as during the surgery.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Stroke volume variation (SVV) was measured for evaluation of volume status
Time Frame: The duration of the measurement was defined from one minute before induction to the end of the surgery
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Stroke volume variation (SVV,%), was monitored using the pressure recording analytic method.
SVV is a parameter used to asses cardiac preload and fluid responsiveness.
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The duration of the measurement was defined from one minute before induction to the end of the surgery
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Pulse pressure variation (PPV) was measured for evaluation of volume status
Time Frame: The duration of the measurement was defined from one minute before induction to the end of the surgery
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Pulse pressure variation (PPV,%) was monitored using the pressure recording analytic method.
PPV is a parameter used to asses cardiac preload and fluid responsiveness
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The duration of the measurement was defined from one minute before induction to the end of the surgery
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Cardiac power output (CPO) was measured for evaluation of cardiac power reserve
Time Frame: The duration of the measurement was defined from one minute before induction to the end of the surgery
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Cardiac power output (CPO, Watt) was monitored using the pressure recording analytic method.
CPO is a parameter used to asses cardiac reserve
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The duration of the measurement was defined from one minute before induction to the end of the surgery
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Cardiac index (CI) was measured for evaluating cardiac flow
Time Frame: The duration of the measurement was defined from one minute before induction to the end of the surgery
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Cardiac index (CI, L/min/m2), was monitored using the pressure recording analytic method.
CI is a parameter used to asses cardiac stroke volume.
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The duration of the measurement was defined from one minute before induction to the end of the surgery
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Dp/Dt was measured to assess cardiac systolic function
Time Frame: The duration of the measurement was defined from one minute before induction to the end of the surgery
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Dp/Dt(mmHg/msn), was monitored using the pressure recording analytic method.
Dp/Dt is a parameter used to asses cardiac contractility.
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The duration of the measurement was defined from one minute before induction to the end of the surgery
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Systolic arterial pressure (SAP) was measured for evaluating perfusion pressure
Time Frame: The duration of the measurement was defined from one minute before induction to the end of the surgery
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Systolic arterial pressure (SAP- mm/Hg) was monitored using the pressure recording analytic method.
SAP is a parameter used to assess the pressure of the arterial system during cardiac systole
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The duration of the measurement was defined from one minute before induction to the end of the surgery
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Diastolic arterial pressure (DAP) was measured for evaluating perfusion pressure
Time Frame: The duration of the measurement was defined from one minute before induction to the end of the surgery
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Diastolic arterial pressure (DAP, mm/Hg) was monitored using the pressure recording analytic method.
DAP is a parameter used to assess the pressure of the arterial system during cardiac diastole
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The duration of the measurement was defined from one minute before induction to the end of the surgery
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Mean arterial pressure (MAP) was measured for evaluating perfusion pressure
Time Frame: The duration of the measurement was defined from one minute before induction to the end of the surgery
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Mean arterial pressure (MAP, mm/Hg) was monitored using the pressure recording analytic method.
MAP is a parameter used to assess organ perfusion
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The duration of the measurement was defined from one minute before induction to the end of the surgery
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Heart rate (HR) was measured for evaluating heart ritm
Time Frame: The duration of the measurement was defined from one minute before induction to the end of the surgery
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Heart rate( HR, bpm) was monitored using the pressure recording analytic method.
HR is a parameter used to assess the cardiac rate
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The duration of the measurement was defined from one minute before induction to the end of the surgery
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Arterial elastance ( Ea) was measured for evaluation of cardiac afterload and arterial ton
Time Frame: The duration of the measurement was defined from one minute before induction to the end of the surgery
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Ea ((mmHg m-2ml-1) was monitored using the pressure recording analytic method.
Ea is a parameter used to assess cardiac afterload and arterial tone
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The duration of the measurement was defined from one minute before induction to the end of the surgery
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The Kidney Disease: Improving Global Outcomes (KDIGO) criteria were used for the definition and staging of acute kidney injury .
Time Frame: The duration of the measurement was defined from the end of the surgery to the 3 days after surgery
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KDIGO criteria ( stage) classify acute kidney injury based on changes in serum creatinine levels and urine output.
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The duration of the measurement was defined from the end of the surgery to the 3 days after surgery
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Fevzi Toraman, M.D., Acibadem Mehmet Ali Aydinlar University School of Medicine, Department of Anesthesiology
Publications and helpful links
General Publications
- Joo EY, Moon YJ, Yoon SH, Chin JH, Hwang JH, Kim YK. Comparison of Acute Kidney Injury After Robot-Assisted Laparoscopic Radical Prostatectomy Versus Retropubic Radical Prostatectomy: A Propensity Score Matching Analysis. Medicine (Baltimore). 2016 Feb;95(5):e2650. doi: 10.1097/MD.0000000000002650.
- Lestar M, Gunnarsson L, Lagerstrand L, Wiklund P, Odeberg-Wernerman S. Hemodynamic perturbations during robot-assisted laparoscopic radical prostatectomy in 45 degrees Trendelenburg position. Anesth Analg. 2011 Nov;113(5):1069-75. doi: 10.1213/ANE.0b013e3182075d1f. Epub 2011 Jan 13.
- Sudfeld S, Leyh-Bannurah SR, Budaus L, Graefen M, Reese PC, von Breunig F, Reuter DA, Saugel B. Impact of perioperative administration of 6 % hydroxyethyl starch 130/0.4 on serum cystatin C-derived renal function after radical prostatectomy: a single-centre retrospective study. BMC Anesthesiol. 2016 Aug 30;16(1):69. doi: 10.1186/s12871-016-0236-8.
- Emir NS, Akyol D, Sabaz MS, Karadag S. Robotic assited perineal prostatectomy (RAPP) as a new era for anesthesiology: It's effects on hemodynamic parameters and respiratory mechanics. J Robot Surg. 2023 Jun;17(3):933-940. doi: 10.1007/s11701-022-01482-x. Epub 2022 Nov 16.
- Valdivieso RF, Hueber PA, Zorn KC. Robot assisted radical prostatectomy: how I do it. Part I: Patient preparation and positioning. Can J Urol. 2013 Oct;20(5):6957-61.
- Karaveli A, Kavakli AS, Cakin O, Aykal G, Yildiz A, Ates M. Comparison of plasma neutrophil gelatinase-associated lipocalin (NGAL) levels after robot-assisted laparoscopic and retropubic radical prostatectomy: an observational study. Braz J Anesthesiol. 2022 Jan-Feb;72(1):21-28. doi: 10.1016/j.bjane.2021.03.003. Epub 2021 Apr 2.
- Pawlik MT, Prasser C, Zeman F, Harth M, Burger M, Denzinger S, Blecha S. Pronounced haemodynamic changes during and after robotic-assisted laparoscopic prostatectomy: a prospective observational study. BMJ Open. 2020 Oct 5;10(10):e038045. doi: 10.1136/bmjopen-2020-038045.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ATADEK 2021-01/2
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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