Comparison Between Two Methods for Renal Stone Treatment Mini Percutaneous Nephrolithotomy and Flexible Ureteroscopy With Suction Sheath

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAin Shams University

About this trial

This study aims to compare the efficacy and safety of two modern, minimally invasive surgical techniques for the removal of kidney stones: Mini-Percutaneous Nephrolithotomy (Mini-PCNL) and Flexible Ureteroscopy (FURS) with Flexible and navigable suction sheath

The primary objective is to determine which procedure results in a higher stone-free rate, as measured by post-operative imaging. Secondary objectives include comparing operative time, hospitalization length andcomplication rates between the two treatment groups.

Patients with two to three centimeter kidney stones who are candidates for either procedure will be randomly assigned to undergo either Mini-PCNL or suctioning FURS. The outcomes will be critically assessed to help establish a higher level of evidence for guiding surgical management of kidney stones.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patients aging 18 years old or more.

Patients with renal stones between 2-3 cm in size confirmed by CT scan.

Disqualifiers

Patients with previous ureteric injury.

Patients with uncontrolled diabetes mellitus or hypertension.

Patients with uncontrolled hepatic dysfunction.

Patients with uremia or renal failure.

Trial design

Design model

Parallel

Treatments tested in this trial

  • mini-percutaneous nephrolithotomy

    Procedure/Surgery

    Under general anesthesia, a 6 Fr ureteral catheter will be placed into the target ureter via cystoscopy, and bladder drainage will be achieved with a 16 Fr Foley catheter. The patient will then be repositioned to the prone position. Percutaneous renal access will be obtained by puncturing the selected calyx with an 18-gauge coaxial needle under fluoroscopic or ultrasound guidance. Tract dilation will be performed using fascial dilators up to 20 Fr then the mini-PCNL sheath (mini-Amplatz sheath) will be inserted and the mini nephroscope 12 to 15 Fr will be used. If multiple nephrostomy tracts are required for stone removal, the same approach will be repeated for each tract. Stone fragmentation will be carried out with a pneumatic lithotripter. At the end of the procedure, a 6 Fr double-J ureteral stent will be inserted for 4 weeks, and whether to place a nephrostomy tube will be determined at the discretion of the operating surgeon.

  • Flexible Uerteroscopy with Tip-Bendable Suction Sheath

    Procedure/Surgery

    under general anesthesia with the patient in the lithotomy position. A 6 Fr ureteral catheter will first be placed into the ureter, followed by retrograde pyelography to assess the upper urinary tract. A guidewire will then be advanced into the renal pelvis. either a 12/14 Fr or 11/13 Fr tip-bendable S-UAS will be inserted. If insertion is not possible due to ureteral narrowing, a smaller 10/12 Fr UAS will be attempted. if failed, a double-J stent will be placed and the procedure terminated, with a second session scheduled 4 weeks later. fURS will be performed using digital flexible ureteroscopes either 8.5 Fr or 7.5 Fr according to UAS size; an 8.5-Fr scope for a 12/14 Fr UAS, and a 7.5-Fr scope for an 11/13-Fr or 10/12-Fr UAS. Stone fragmentation will be performed using a holmium laser (Ho: YAG) with a 272-μm fiber and an energy setting below 30 W. Irrigation will be maintained at 50-100 ml/min and suction pressure at 80-120 mmHg. at the end a 6 Fr JJ will be inserted for 4 weeks.

Treatment groups

120 Participants
are divided into 2 treatment groups
Group A: mini-PCNLExperimental treatment 1 intervention
Group B: FURS with Tip-Bendable Suction SheathExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

stone free rate

The proportion of participants in each treatment arm who are completely free of any stone fragments in the treated kidney, following the initial procedure and without the need for any secondary surgical interventions. Status will be determined by a blinded central radiologist.

Time frame
one month postoperative

Secondary outcomes

1

length of hospital stay

The total duration of inpatient hospitalization following the procedure, calculated from the day of surgery to the day of discharge

Time frame
From date of surgery until date of hospital discharge for 14 days (measured in days).
2

operative time

The total time from the initiation of the procedure to the final removal of all endoscopic equipment and placement/completion of any necessary stents

Time frame
Measured intraoperatively, from procedure start to end (in minutes).

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Ain Shams University

Lead sponsor

Ahmed Maher Teaching Hospital

Sponsor institution