About this trial
This study aims to evaluate the changes between preoperative and postoperative serum chloride levels in patients undergoing HoLEP surgery and to investigate the metabolic and clinical effects of this change. The study is observational, and no additional interventions will be performed.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patients scheduled for elective HoLEP surgery.
Patients providing written informed consent
Disqualifiers
Preoperative metabolic acidosis.
Advanced renal failure.
Emergency surgery.
Missing data.
Trial population
Patients scheduled for elective HoLEP surgery.
Trial design
Cohort
Prospective
Treatments tested in this trial
HoLEP surgery
Procedure/SurgeryAll parameters are part of routine clinical practice; no additional examinations are required
Treatment groups
Trial outcomes
Primary outcomes
Change in serum chloride level
Secondary outcomes
irrigation volume
Arter blood gas
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: