Metabolic and Clinical Effects of Hyperchloremia During HoLEP Surgery.

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age18+
SponsorAnkara City Hospital Bilkent

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • HoLEP surgery

    Procedure/Surgery

    All parameters are part of routine clinical practice; no additional examinations are required

Treatment groups

45 Participants
are divided into 1 treatment group
Group A: Patients undergoing elective HoLEP surgery.1 intervention

Trial outcomes

Primary outcomes

1

Change in serum chloride level

Time frame
Perioperative

Secondary outcomes

1

irrigation volume

Time frame
Perioperative
2

Arter blood gas

Time frame
Perioperative

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: