Skip to content

sterile water and normal saline in PCNL

comparison of efficacy and adverse effects of sterile water and normal saline for irrigation fluid in percutneous nephrolithotripsy(PCNL)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201212291323N5
Enrollment
94
Registered
2013-02-11
Start date
2011-06-01
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

Calculus of kidney with calculus of ureter. Calculus of kidney with calculus of ureter

Interventions

Intervention 1: Case group :use of sterile water as an irrigation fluid during PCNL operation. Intervention 2: control group :use of normal saline as an irrigation fluid during PCNL operation.
Treatment - Surgery
Case group :use of sterile water as an irrigation fluid during PCNL operation
control group :use of normal saline as an irrigation fluid during PCNL operation

Sponsors

Deputy of information and Research , Yasuj University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: inclusion and exclusion criteria are includes (Inclusion criteria:Age>18 years old ,patients with renal or upper ureteral stone larger than 20 millimeter candidate for percutaneous nephrolithotripsy , Exclusion criteria: patients with urinary stone younger than 18 years old ,patients with azotemia.uncontrolled coagulopathy,active infection,history of hemolysis,any contraindication for general or spinal anesthesia,COPD,ASA score 3 and 4 )

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Cheke of serum electrolytes and hemolysis in percutaneous nephrolithotripsy. Timepoint: Before operation and 6 hour after operation. Method of measurement: checking Na,K,and serum haptoglubin before and 6 hour operation.

Secondary

MeasureTime frame
Development of any cardiovascular or pulmonary complications. Timepoint: during operation to one week later. Method of measurement: report of patients and observation with examination lung and heart of of patients pulse oximetery during operation,and check of lower limb pulses.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Sadrollah Mehrabi

Social Health Determinant of research center,Yasuj university of medical science

sadrollahm@yahoo.com and dr mehrabiyums.ac.ir+98 74 1222 1813

Outcome results

None listed

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