Percutaneous Nephrolithotomy Without a Ureteral Catheter

Sponsor
The First Affiliated Hospital of University of South China (Other)
Overall Status
Recruiting
CT.gov ID
NCT05598671
Collaborator
(none)
200
1
2
27
7.4

Study Details

Study Description

Brief Summary

Conventional Percutaneous nephrolithotomy (PCNL) surgery requires the patient to first undergo retrograde transurethral ureteroscopic insertion of the ureteral catheter in the lithotomy position, and then change the patient to the prone position. However, repeated operation on the ureter can bring about immediate and long-term negative effects, such as ureteral false way formation, ureteral damage, perforation, avulsion, catheter insertion into the vena cava, pricking the kidney, increased postoperative pain, urinary extravasation, scar formation, and ureteral narrowing. The study planned to perform the operation in the prone position without reverse insertion of a ureteral catheter in the PCNL surgery.

Condition or Disease Intervention/Treatment Phase
  • Procedure: PCNL without reverse insertion of a ureteral catheter
N/A

Detailed Description

The purpose of this single-center, single-blind, randomized trial was to evaluate the safety and efficacy of PCNL without reverse insertion of a ureteral catheter. It is planned to start in November 2022 and is expected to end in November 2024. Based on inclusion and exclusion criteria, 200 subjects were expected to be recruited. In a parallel group design, subjects were randomly assigned to two groups: the experimental group received PCNL without reverse insertion of a ureteral catheter , and the control group received traditional PCNL. The primary end point of the study was the incidence of postoperative complications according to the modified Clavien-Dindo complication grading system. Secondary end points included Stone-free rate, operation time, length of hospital stay, and medical costs. Measurement data were expressed as mean ± standard deviation (X ± S), and Student's t-test was used for intergroup comparisons. The counting data were expressed as frequency and percentage, and the chi-squared or Fisher's exact probability test were used for intergroup comparisons. The rank-sum test was used for grade data. P<0.05 was considered statistically significant.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
A Comparative Study of Retrograde Ureteral Catheter Insertion or Not in Percutaneous Nephrolithotomy
Actual Study Start Date :
Nov 3, 2022
Anticipated Primary Completion Date :
Nov 1, 2024
Anticipated Study Completion Date :
Feb 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: without reverse insertion of a ureteral catheter

Percutaneous nephrolithotomy without reverse insertion of a ureteral catheter

Procedure: PCNL without reverse insertion of a ureteral catheter
The ureteral catheter was not retrograde inserted during PCNL

No Intervention: Conventional

Percutaneous nephrolithotomy with reverse insertion of a ureteral catheter

Outcome Measures

Primary Outcome Measures

  1. Rate of fever [From the day of surgery to the day of discharge, up to 2 weeks.]

    Fever was defined as axillary temperature greater than 38.5 ° C.

  2. White blood cell count change value [Day 2 before surgery、hour 3 after the surgery]

    The change value of White blood cell count between preoperative and postoperative

  3. Neutrophils granulocyte change value [Day 2 before surgery、hour 3 after the surgery]

    The change value of Neutrophils granulocyte between preoperative and postoperative

  4. Hemoglobin change value [Day 2 before surgery、hour 3 after the surgery]

    The change value of Hemoglobin between preoperative and postoperative

  5. Hematocrit change value [Day 2 before surgery、hour 3 after the surgery]

    The change value of Hematocrit between preoperative and postoperative

  6. Rate of renal subcapsular hematoma [Day 2 after the surgery]

    The proportion of postoperative renal subcapsular hematoma in all patients

  7. Serum creatinine change value [Day 2 before surgery、Hour 3 after the surgery]

    The change value of Serum creatinine between preoperative and postoperative

  8. visual analog scale (VAS)pain score [Hour 2 after the surgery]

    0: no pain; Less than 3 points: mild pain, tolerable; 4 points to 6 points: the patient's pain and affect sleep, still tolerable; 7-10: Patients have increasing pain, pain is unbearable, affect appetite, affect sleep.

  9. Rate of hydrothorax [Day 2 after the surgery]

    Hydrothorax appeared on the surgical side.

Secondary Outcome Measures

  1. Stone free rate [Day 2 after the surgery]

    Residual stone less than 4mm in diameter was considered to have been cleared.

  2. Operation time [During the procedure]

    Operation time was defined as the time required from the surgeon's handwashing to the completion of surgical incision suture

  3. length of hospital stay [2 weeks after surgery]

    Length of hospital stay indicated the number of days between the operation date and discharge date

  4. Medical costs [2 weeks after surgery]

    All medical expenses incurred to treat stones.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

· Patients with upper urinary tract stones who were 18 years of age or older and eligible for PCNL surgery.

Exclusion Criteria:
  • patients with infectious calculi confirmed by preoperative CT examination and blood biochemical indexes.

  • Patients with severe cardiac and pulmonary insufficiency, coagulation dysfunction and other obvious surgical contraindications.

  • Patients with previous history of PCNL surgery on the affected side or nephrotomy.

  • Patients with indwelling double J tube or nephrostomy tube before operation.

  • Patients with renal trauma or congenital anomalies of urinary system.

Contacts and Locations

Locations

Site City State Country Postal Code
1 The First Affiliated Hospital of University of South China Hengyang Hunan China 421001

Sponsors and Collaborators

  • The First Affiliated Hospital of University of South China

Investigators

  • Study Director: Mingyong Li, MD., the First Affiliated Hospital of the University of South China

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Li Mingyong, MD, Associate professor, The First Affiliated Hospital of University of South China
ClinicalTrials.gov Identifier:
NCT05598671
Other Study ID Numbers:
  • nhfy0520
First Posted:
Oct 28, 2022
Last Update Posted:
Dec 7, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 7, 2022