ClinicalTrials.gg
Not yet recruitingNCT07510178Updated Apr 15, 2026

Retrograde Intrarenal Surgery Versus Extracorporeal Shockwave Lithotripsy

An interventional study of Retrograde intrarenal surgery and Extracorporeal shock wave lithotripsy in Renal Stone and Stone in Calyceal Diverticulum, sponsored by Sindh Institute of Urology and Transplantation. Not yet recruiting at 1 site in Pakistan. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2026-04-15.

Sponsored by Sindh Institute of Urology and Transplantation · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
66
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

The study's aim is to determine which treatment modality, either ESWL or RIRS, is more effective in achieving stone clearance for lower calyceal calculi.

Investigators hypothesize that retrograde intrarenal surgery is better as compared to extracorporeal shockwave lithotripsy. It will target those patients suffering from kidney stones in lower calyces with sizes up to 1.5 cm in an open-label, randomized controlled trial.

Read the detailed description

After approval from the Institutional Ethical Review Committee and taking informed consent from the patients, the investigator will gather all the information related to the study. Patients will be enrolled in this study from the outpatient clinic. Total patients will be divided into two groups using the SNOSE protocol, in which patients will be randomly assigned to one of the two groups using the envelope method.

Group A will be labeled under those patients who will be treated by ESWL. Group B will be those treated by RIRS. It will be an open-label study. A Performa has been designed and finalized after a literature search. This form will gather demographic details, clinical characteristics, selection of procedure, procedure details, outcomes of procedure, and complications.

In case of ESWL, up to 3 sessions of ESWL will be given, and for RIRS, only one session will be considered. In ESWL, ultrasound- or fluoroscopy-guided 3000 shock waves per person are delivered under the supervision of an experienced consultant urologist for up to 60 - 90 minutes using lithotripsy model SLX-F2 FD21 with energy ranging from 1 to 6, and patients are discharged on proper hydration, painkillers, and alpha blockers. In RIRS, firstly, a retrograde pyelogram is performed to know the anatomy and stone position. Then, using aseptic technique, a sterile flexible 7.5/3.6 Fr ureterorenoscope of model HU30S will be passed over a Y-9-50 ureteral access sheath and advanced into the kidney, and the stone will be broken with the use of a 35-watt hyperphotonic holmium laser delivered via a 272 nm fiber. The RIRS will be performed by an experienced urologist. Later patients will be discharged with advice of hydration and empirical antibiotics. Initially the stone bulk will be defined by a CT scan, and the Hounsfield unit of stones will be noted. The infundibular pelvic angle, calyx length, diameter, and skin-to-stone distance will also be calculated using the CT scan plane. Patients managed either by RIRS or ESWL will be advised for a follow-up after four weeks with an X-ray KUB for radiopaque stones and an ultrasound and CT scan of the kidneys to look for residual radiolucent calculi. Stone clearance will be considered if residual stone size is less than 4 mm.

02

Conditions studied

  • Renal Stone
  • Stone in Calyceal Diverticulum

Browse trials for

Keywords

  • renal stone
  • lithotripsy
  • retrograde
03

In context

Nephrolithiasis

324 studies on the registry are indexed under Nephrolithiasis; 90 are open to participants now.

This study's planned enrollment of 66 is below the median of 92 across 257 interventional studies indexed under Nephrolithiasis.

Browse Nephrolithiasis studies →

Lead sponsor

Sindh Institute of Urology and Transplantation is the lead sponsor of 18 studies on the registry; 6 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Those patients will be included with lower calyceal renal stones and size up to 1.5 cm.
  • Patients' ages will be between 18 and 60 years.
  • Both genders will be included.

Exclusion criteria

Exclusion Criteria:

  • Untreated Urine culture positive will be excluded
  • Patients using anticoagulants and females with pregnancies and those lactating will be excluded.
  • Anatomical abnormalities like horseshoe kidney, duplex system, pelvic kidney, malrotated kidney, calyceal diverticulum, steep infundibulopelvic angle, infundibular stenosis, long infundibular length/narrow infundibular width, pelvic ureteric junction obstruction, ureterocele, and ureteral stricture will be excluded.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
66 participants (estimated)

Study arms

  • Active comparator
    Group A

    Group A will be comprised of those patients who will be treated by ESWL (shockwave lithotripsy).

    Procedure: Extracorporeal shock wave lithotripsy

  • Experimental
    Group B

    Group B will be comprised of those patients who will be treated by RIRS (retrograde intrarenal surgery).

    Procedure: Retrograde intrarenal surgery

Interventions

  • ProcedureRetrograde intrarenal surgery

    Retrograde intrarenal surgery (RIRS) is a minimally invasive procedure in which a flexible ureteroscope is passed through the urethra, then the ureter, and then into the kidney, and then with the help of the laser, stones are broken down into small fragments, which can be retrieved either at the same time or flushed later in urine. Stone clearance will assessed with an X-ray of the abdomen (radiopaque) and ultrasound or CT scan of the kidneys (residual radiolucent stones) on follow-up.

  • ProcedureExtracorporeal shock wave lithotripsy

    Extracorporeal shock wave lithotripsy (ESWL) is a noninvasive procedure in which highly focused shock waves are delivered at the renal calculi, which then break down into small pieces and later pass in urine. An X-ray abdomen (radiopaque) and ultrasound or CT scan of the kidneys (residual radiolucent stone) will be used on follow-up to assess stone clearance. Up to 3 sessions of ESWL will given to the selected candidate

06

What researchers measure

Primary outcomes

  1. Stone clearance

    Stone clearance (based on follow-up with X-Ray for radio-opaque stones and ultrasound or CT Scan for radio-lucent stones)

    Time frame: four weeks after the intervention

Secondary outcomes

  1. Urinary tract infection

    It is diagnosed if the patient starts complaining of burning micturition along with a running temperature. It will be confirmed by a urine D/R with a culture \& sensitivity report.

    Time frame: within 4 weeks after the intervention

  2. Hematuria

    It will be diagnosed if the patient starts complaining of burning micturition along with red discoloration of urine. It will be confirmed by the presence of numerous RBCs in a urine D/R

    Time frame: within 4 weeks after the intervention

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No — Only results will be shared

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07510178
Lead sponsor
Sindh Institute of Urology and Transplantation
Responsible party
Maaz Bin Nazir (Resident, Sindh Institute of Urology and Transplantation) — Principal investigator
First posted
Apr 3, 2026
Start date
Apr 30, 2026 (estimated)
Primary completion
Oct 30, 2026 (estimated)
Completion
Oct 30, 2026 (estimated)
Last update
Apr 15, 2026

Study contacts

Maaz Nazir
Contact
maazbinnazir@yahoo.com
+923122949655
Abdul Khaliq, FCPS
study director · Sindh Institute of Urology and Transplantation

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion