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Evaluation of Renal Perfusion With NIRS in Laparoscopic Surgery

D

Diskapi Yildirim Beyazit Training and Research Hospital

Status

Not yet enrolling

Conditions

Pneumoperitoneum
Renal Injury

Treatments

Device: NIRS

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The investigators aimed to show the renal damage caused by increased intra-abdominal pressure in laparoscopic surgeries and to investigate whether its reflection on NIRS would be clinically effective.The main question it aims to answer are:

Does pneumoperitoneum cause renal damage?

NRS monitoring will be performed in patients undergoing laparoscopic surgery. Preoperative and postoperative blood tests will be performed at certain hours. N-GAL, urea and creatinine values will be recorded.

Full description

Renal NIRS monitoring will be performed in patients undergoing laparoscopic cholecystectomy surgery. Age, gender, BMI, ASA scores, hemogblin/hematocrit values, intraoperative hemodynamic parameters, NIRS values, N-GAL (preoperative, 2nd hour and 24th hour), urea/creatinine (preoperative, postoperative 24th hour) values of the patients will be recorded. .

Before the general anesthesia is performed, the renal tissues of the patients will be visualized by ultrasound, the skin-renal cortex distances will be measured, and suitable patients will be included in the study. Basal rSO2 values will be recorded by placing NIRS probes under the 10-11. intercostal space in the bilateral posterior lateral flank region.

Enrollment

58 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who undergoing elective laparoscopic cholecystectomi surgery lasting longer than 60 minutes
  • BMI:18-25
  • skin-renal cortex distance measured less than 4 cm on ultrasound
  • ASA I-III

Exclusion criteria

  • patient who did not give consent
  • patient who had renal operation before,
  • infection, abscess, catheter in the perirenal region
  • hemodynamically unstable patients,
  • patients with renal pathology and abnormal kidney function tests,
  • emergency cases

Trial design

58 participants in 1 patient group

Patients undergoing laparoscopic cholecystectomy.
Description:
Basal rSO2 values will be recorded by placing NIRS probes under the 10-11th intercostal space in the bilateral posterior lateral flank region. Age, gender, BMI, ASA scores, Hb/Htc values, intraoperative hemodynamic parameters, NIRS values, N-GAL (preoperative, 2nd hour and 24th hour), urea/creatinine (preoperative, postoperative 24th hour) values of the patients will be recorded. .
Treatment:
Device: NIRS

Trial contacts and locations

1

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Central trial contact

Savaş Altınsoy, MD

Data sourced from clinicaltrials.gov

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