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NCT Number: NCT05574517

Tubeless Percutaneous Nephrolithotomy Without Reverse Insertion of a Ureteral Catheter

Percutaneous nephrolithotomy(PCNL) is a surgical method for upper urinary calculi. The advent of tubeless PCNL (without indwelling nephrostomy tube) has been proved to be safe and effective in reducing postoperative discomfort, shortening hospitalization time and reducing hospitalization costs. Traditional tubeless PCNL usually involves retrograde insertion of the ureteral catheter, which may cause many ureteral related surgical complications. However, there are few reports on tubeless PCNL without reverse ureteral catheter insertion. The goal of this study is to explore the safety and effectiveness of the tubeless PCNL without reverse ureteral catheter insertion.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The First Affiliated Hospital of University of South China

Hengyang, Hunan, 421001, China

Location status: Recruiting

Location contact

Mingyong LI

CONTACT

[email protected]

18175878363

About this study

This is a key clinical research project of the University of South China (No. USCKF201902K01). The goal of this study is to comparative the safety and clinical efficacy between the tubeless percutaneous nephrolithotomy without reverse insertion of a ureteral catheter and the traditional tubeless percutaneous nephrolithotomy with reverse insertion of a ureteral catheter in the treatment of upper urinary calculi, and to explore the former' applications. It is a prospective, randomized controlled single center study that is conducted for 2 years anticipatively. The clinic physician is responsible for patient recruitment and allocation and the application of computerized random-number generation. For random allocation, participants are given random numbers. Participants with odd numbers are assigned to experimental group, where they undergo tubeless PCNL without reverse insertion of a ureteral catheter. Participants with even numbers are assigned to control group and undergo tubeless PCNL with reverse insertion of a ureteral catheter. The doctors managing the operations accept participants and execute the surgical treatments. All participants sign clinical-trial informed consent and surgical informed consent during the preoperative conversation. Follow-up observation is conducted for 1 month after surgery. After completion of the study, we collect relevant clinical data from the participants. The primary and secondary outcomes are analyzed and compared between the two groups.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants who met the the applications of PCNL surgery in the 2019 Chinese Guidelines for the Diagnosis and Treatment of Urological Diseases
  • Participants who agree to undergo tubeless PCNL
  • The participants' maximum diameter of the stone should be less than 3.5cm

Exclusion criteria

  • Confirmation by computerized tomography (CT) images and blood biochemical indicators of infectious stones or complex staghorn stones
  • Obvious surgical contraindications, such as severe heart and lung insufficiency, abnormal coagulatory function
  • Previous PCNL or nephrolithotomy, presence of an indwelling ureteral stent or nephrostomy tube before surgery
  • Renal trauma or congenital malformation of the urinary system

Treatment and study plan

Without reverse insertion of a ureteral catheter

Procedure

Traditional tubeless percutaneous nephrolithotomy usually need retrograde ureteral catheter insertion. Our intervention is that the tubeless percutaneous nephrolithotomy is executed without reverse insertion of a ureteral catheter.

Primary outcomes

  1. Changes of inflammatory indicators after surgery

    Time frame: Hour 3 after the surgery

    Pre- vs. post-operative blood leukocyte counts and neutrophil-ratio difference

  2. Changes in renal bleeding after surgery

    Time frame: Hour 3 after the surgery

    Pre- vs. post-operative difference in hemoglobin and hematocrit values

  3. Changes of renal-function after surgery

    Time frame: Hour 3 after the surgery

    Preoperative and postoperative blood creatinine difference

  4. Pain score after surgery

    Time frame: Hour 3 after the surgery

    According to the Visual Analogue Scale(VAS) to evaluate the score. Scores range from 0 to 10, where 0 represents no pain and 10 represents the highest pain.

  5. Incidence of pneumothorax and hydrothorax

    Time frame: Day 2 after the surgery

    The rate of pneumothorax and hydrothorax after surgery

  6. Incidence of ureteral stone street

    Time frame: Day 2 after the surgery

    The rate of ureteral stone street after surgery

Secondary outcomes

  1. Duration of operation

    Time frame: during the procedure

    From the completion of anesthesia to the end of the suture incision.

  2. Duration of hospital stay

    Time frame: immediately after the discharge

    From the date of admission to the date of discharge.

  3. Hospital costs

    Time frame: immediately after the discharge

    The cost from hospitalization to discharge.

  4. Stone-free rates

    Time frame: Day 2 after the surgery

    Preoperative and postoperative stone dimensions are compared by radiological assessment. Postoperative residual calculi < 4 mm in diameter reflect complete removal of calculi (stone-free rate = 100%).

Study contacts

Contact information is provided by the study sponsor or research team.

Mingyong Li, MD

CONTACT

[email protected]

18175878363

Sponsors and collaborators

Lead sponsor

The First Affiliated Hospital of University of South China

Other

Registry information

Official study title

A Comparative Study of Tubeless Percutaneous Nephrolithotomy With or Without Reverse Ureteral Catheter Insertion

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
Oct 10, 2022
Registry last updated
Sep 24, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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