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Comparing efficacy and safety of conventional and totally tubeless percutaneous nephrolithotomy in under 14 year-old patients; a clinical trial

Comparing efficacy and safety of conventional and totally tubeless percutaneous nephrolithotomy in under 14 year-old patients; a clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201110017675N1
Enrollment
20
Registered
2011-10-08
Start date
2010-07-01
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Kidney stone. Calculus of kidney

Interventions

Intervention 1: intervention: Totally tubeless percutaneous nephrolithotomy. Intervention 2: control: standard percutaneous nephrolithotomy.
Treatment - Surgery
intervention: Totally tubeless percutaneous nephrolithotomy
control: standard percutaneous nephrolithotomy

Sponsors

Vice chancellor for research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 14 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria were patient age less than 14 years old; the existence of stone size >2.5 cm; stone resistant to extracorporeal shockwave lithotripsy (SWL). The exclusion criteria were serious bleeding; perforation in the collecting system during the operation; kidney anomalies; renal failure on admission.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Postoperative analgesic requirement. Timepoint: after surgery till discharge. Method of measurement: mg of morphine use.;Hospitalization period. Timepoint: after surgery till discharge. Method of measurement: days of hospitalization.

Secondary

MeasureTime frame
Operation time. Timepoint: time of surgery. Method of measurement: minutes of surgery.;Hemoglobin changes. Timepoint: during surgery till discharge. Method of measurement: mg/dl of Hemoglobin.;Need to re-operation. Timepoint: after surgery, 1 week and 1 month later. Method of measurement: need to re-operation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi Aloosh

Tehran University of Medical Sciences

m_aloosh@farabi.tums.ac.ir+98 21 6634 8556

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026