Effect of Renal Access Sheath on Functions

Sponsor
Bakirkoy Dr. Sadi Konuk Research and Training Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05232188
Collaborator
(none)
88
1
2
21
4.2

Study Details

Study Description

Brief Summary

Patients will be randomly divided into two groups in order to evaluate the effect of the size of the access sheath (Amplatz) used in the Percutaneous Nephrolithotomy (PCNL) operation on kidney functions. After dilatation, 22French (Fr) Amplatz sheath will be placed in the first group, while 28Fr Amplatz sheath will be placed in the second group.

The functional difference will be evaluated with preoperative and postoperative 3rd-month kidney scintigraphies (diethylenetriamine pentaacetic acid (DTPA) and technetium-99m dimercaptosuccinic acid (DMSA). In addition, Kidney Injury Molecule-1 (KIM-1) levels will be measured in the urine in order to be a predictor of functional loss in the early period.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Percutaneous nephrolithotomy
N/A

Detailed Description

PCNL has been applied for the last 30 years as the primary and most effective treatment method in patients with kidney stones of 2 cm or larger. The primary purpose of the operation is to ensure stone-freeness. Another aim is to keep the damage to kidney functions to a minimum, thanks to the endoscopic intervention. In this respect, PCNL is superior to open surgery and reduces morbidity.

Renal access, dilatation, and fragmentation are the 3 important stages of the operation, and access and dilation significantly affect the final results of PCNL. The size of the access sheath used as a result of dilation determines the size of the tract where the endoscopic intervention will be made, and not only affects the postoperative results and success but also determines the factors that may affect the kidney functions such as bleeding and loss of parenchyma in the kidney.

There are studies showing that less bleeding, shorter hospital stay, and better postoperative pain control are achieved with the reduction of access sheath size. In addition to conventional PCNL, methods such as mini PCNL, micro PCNL, ultra-mini PCNL, and tubeless PCNL, where the diameter of the access sheath and endoscope are gradually decreasing, both increase success and reduce morbidity.

In our study, in order to examine the postoperative functional results of 22 Fr and 28 Fr accessory sheath size;

  • For the early period, the change in KIM-1 values, a validated biomarker in acute kidney injury, measured on the preoperative and postoperative day 1 will be proportioned between the groups,

  • For the late period, we aimed to compare the kidney functions in the mid-long term by proportioning the DMSA and DTPA values at the preoperative and postoperative 3rd month.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
88 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Effect of Renal Access Sheath Size Used During Percutaneous Nephrolithotomy on Postoperative Renal Functions
Actual Study Start Date :
Dec 1, 2020
Anticipated Primary Completion Date :
Jul 1, 2022
Anticipated Study Completion Date :
Sep 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: 22French (Fr)

After renal access, dilatation is provided up to 22Fr with a dilatator set, and fragmentation is started with a 19Fr nephroscope.

Procedure: Percutaneous nephrolithotomy
percutaneous nephrolithotomy surgery, 22F amplatz sheath is used in one group, while 28F amplatz sheath is used in the other group.

Experimental: 28F

After renal access, dilatation is provided up to 28Fr with a dilatator set, and fragmentation is started with a 25Fr nephroscope.

Procedure: Percutaneous nephrolithotomy
percutaneous nephrolithotomy surgery, 22F amplatz sheath is used in one group, while 28F amplatz sheath is used in the other group.

Outcome Measures

Primary Outcome Measures

  1. Differential function changes [3 months]

    Differential function changes in the operated kidney in postoperative DMSA and DTPA

  2. Newly developed scar [3 months]

    Presence of newly developed scar in DMSA

  3. KIM-1 [24 hours]

    Change in urinary KIM-1 levels

Secondary Outcome Measures

  1. Creatinine [24 hours]

    Postoperative changes in creatinine

  2. Glomerular filtration rate [24 hours]

    Postoperative changes in glomerular filtration rate

  3. Stone-free rate [24 hours]

    Postoperative stone-free rates

  4. Complications [30 days]

    Complications according to Clavian grading

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with 2-3 cm kidney stones

  • Patients with an American Society of Anesthesiologists ≤2 score

  • BMI: Patients between 20 and 35 kg/m2

Exclusion Criteria:
  • Patients with preoperative renal failure

  • Patients with multiple access

  • Patients undergone renal transplantation

  • Patients with renal anomalies (horseshoe kidney, solitary kidney, double collecting system, etc.)

  • Patients with history of open kidney stones surgery and/or PCNL history

  • Patients who cannot be stone-free in the postoperative period (fragments >4 mm in imaging) and require additional treatment intervention

  • Patients with bleeding disorders

  • Pregnant patients

  • Patients with complete staghorn stones

  • Patients with bilateral obstructive stones

  • Patients with active infection

Contacts and Locations

Locations

Site City State Country Postal Code
1 Bakırköy Dr. Sadi Konuk Training and Research Hospital Istanbul Turkey

Sponsors and Collaborators

  • Bakirkoy Dr. Sadi Konuk Research and Training Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
ClinicalTrials.gov Identifier:
NCT05232188
Other Study ID Numbers:
  • NoyanOzluPCNL
First Posted:
Feb 9, 2022
Last Update Posted:
Jun 10, 2022
Last Verified:
Jun 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Bakirkoy Dr. Sadi Konuk Research and Training Hospital

Study Results

No Results Posted as of Jun 10, 2022