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The effect of preoperative intravenous mannitol injection in reducing acute kidney injury following percutaneous nephrolithotomy

The effect of preoperative intravenous mannitol injection in reducing acute kidney injury following percutaneous nephrolithotomy

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200110046073N1
Enrollment
150
Registered
2020-03-01
Start date
2020-03-04
Completion date
Unknown
Last updated
2020-03-24

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

Conditions

Acute kidney injury, Renal stone, Percutaneous nephrolithotomy (PCNL). Postprocedural (acute) (chronic) kidney failure

Interventions

Intervention 1: Intervention group: Interavenous injection of 25 grams of mannitol (125 cc of 20% mannitol Serum) in 75 patients candidated for percutaneous nephrolithotomy, 15 minutes before surgery.

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients with renal stone greater than 20 mm in diameter who are candidated for percutaneous nephrolithotomy. Patients with proximal ureter stone greater than 20 mm in diameter who are candidated for percutaneous nephrolithotomy.

Exclusion criteria

Exclusion criteria: Heart failure History of lung embolism History of deep vein thrombosis History of brain edema History of intracranial hemorrhage Respiratory edema Anuria History of digoxin consumption History of Lithium consumption History of allergy to mannitol Electrolite imbalance Coagolopathies

Design outcomes

Primary

MeasureTime frame
Post percutaneous nephrolithotomy glomerular filtration rate changes. Timepoint: The day before surgery, 6 hours after surgery, 1, 2, and 14 days after surgery. Method of measurement: cockroft gault equation (based on serum creatinine level).

Secondary

MeasureTime frame
Post operative hemoglobin changes. Timepoint: The day before surgery, 6 hours after surgery, 1, 2, and 14 days after surgery. Method of measurement: Complete blood count.;Post operative infection. Timepoint: The day before surgery, 6 hours after surgery, 1, 2, and 14 days after surgery. Method of measurement: Thermometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKaveh Mehravaran

Iran University of Medical Sciences

Mehravarankaveh@yahoo.com+98 21 8864 4441

Outcome results

None listed

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