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Consol Time and Acute Kidney Injury in Robotic-assisted Prostatectomy

NCT06000098 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 42

Last updated 2024-02-02

No results posted yet for this study

Summary

Robotic-assisted laparoscopic prostatectomy (RALP) is the gold standard surgical technique in prostate surgery. Many Robotic-laparoscopic surgical techniques also require the intraoperative deep Trendelenburg position and intravenous fluid restriction during surgery. However, the possible side effects of the deep Trendelenburg's position and the fluid restriction on the cardiovascular and renal systems during surgery are unknown. Although the Trendelenburg position is a life-saving maneuver in hypovolemic patients, it also carries undesirable risks. Long console time may contribute to the development of acute kidney injury (AKI) by prolonging the Trendelenburg time and the fluid-restricted time. In this study, investigators aimed to demonstrate the effect of console time on the development of AKI. Investigators also aimed to determine the hemodynamic risk factors that cause the development of AKI in patients monitored with the pressure Recording Analytical Method (PRAM).

Conditions

Interventions

OTHER

Restrictive fluid therapy

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).

Sponsors & Collaborators

  • Acibadem University

    lead OTHER

Principal Investigators

  • Fevzi Toraman, M.D. · Acibadem Mehmet Ali Aydinlar University School of Medicine, Department of Anesthesiology

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-09-25
Primary Completion
2023-10-15
Completion
2023-10-16

Countries

  • Turkey (Türkiye)

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06000098 on ClinicalTrials.gov