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Renal Stone DiseaseNCT07800546

Intrarenal Pressure Monitoring During Pediatric Percutaneous Nephrolithotomy, and Its Impact on Post Operative Infectious Complications.

A study testing Intrarenal pressure in people with Renal Stone Disease, run by Assiut University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record

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Trial summary

Monitoring of intrarenal pressure during pediatric percutaneous nephrolithotomy and its impact on post operative infectious complications. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Renal Stone Disease
What is being tested?
Intrarenal pressure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
80 participants
Where
No sites listed yet
Study dates
1 Sep 2026to 1 May 2028
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • age < 18 years Undergoing PCNL for renal calculi

Who cannot join

  • Active untreated urinary infection High grade vesicoureteric reflux ( grade IV _V) Immunocompromised patients

About this study

Monitoring of intrarenal pressure during pediatric percutaneous nephrolithotomy and its impact on post operative infectious complications.

Being tested
Intrarenal pressure

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Intrarenal pressureDiagnostic test

    Monitoring of intrarenal pressure during pediatric percutaneous nephrolithotomy

Study groups in NCT07800546
Study groupRoleWhat they receive
Pediatric PCNLActive comparatorIntrarenal pressure during pediatric percutaneous nephrolithotomy
Receives: Diagnostic Test: Intrarenal pressure

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Infectious complications

    Post operative infectious complications after pediatric percutaneous nephrolithotomy

    Measured: 72 hours post operative

  2. Post operative infectious complications

    Monitoring of intrarenal pressure during pediatric percutaneous nephrolithotomy and its impact on post operative infectious complications

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Sep 2026
  2. Study start1 Sep 2026 (estimated)
  3. Primary completion1 Apr 2028 (estimated)
  4. Study completion1 May 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07800546
Sponsor's protocol ID
IRP during pediatric PCNL
Status last verified
Aug 2026
First submitted
29 Aug 2026
Last updated
2 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

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