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Evaluation of the changes of blood pressure, serum sodium and potassium levels after percutaneous nephrolithotripsy surgery

Not Applicable
Conditions
Calculus of kidney.
Calculus of kidney
Registration Number
IRCT2014031116948N1
Lead Sponsor
Vice Chancellor for Research and Technology, Ahvaz Jundishapur University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
63
Inclusion Criteria

The inclusion criteria are the age between 15 to 65 years, having normal levels of sodium and potassium, having a kidney stone with a diameter greater than 2 cm and having 1 and 2 risk of anesthesia. Exclusion criteria include having histories of hypertension, diabetes mellitus, ischemic heart disease, renal failure, hyponatremia and hypokalemia and using drugs that affect serum electrolyte. Also, the change in the performing procedure that lead to more absorption of washing liquid is another exclusion criteria.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Serum level of sodium. Timepoint: before, every 60 minutes during intervention, after the end of the intervention and during the 24 hours post intervention. Method of measurement: meq/L, Laboratory kit.;Serum level of potassium. Timepoint: before, every 60 minutes during washing, after the end of the intervention and during the 24 hours post intervention. Method of measurement: meq/L- Laboratory kit.
Secondary Outcome Measures
NameTimeMethod
Systolic blood pressure. Timepoint: before, every 60 minutes during intervention, after the end of the intervention and during the 24 hours post intervention. Method of measurement: mmHg, by using blood pressure measurement device.;Diastolic blood pressure. Timepoint: before, every 60 minutes during intervention, after the end of the intervention and during the 24 hours post intervention. Method of measurement: mmHg, by using blood pressure measurement device.;Percent of arterial blood oxygen saturation. Timepoint: before, every 60 minutes during intervention, after the end of the intervention and during the 24 hours post intervention. Method of measurement: Percent, by laboratory test.;Heart rate. Timepoint: before, every 60 minutes during intervention, after the end of the intervention and during the 24 hours post intervention. Method of measurement: the number of heartbeat per minute, by hemodynamic monitoring device.
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