About this trial
The aim of this study is to evaluate the efficacy of spinal anesthesia as an alternative to general anesthesia in PCNL operation in supine position.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age more than 21 years old.
Both sexes.
American Society of Anesthesiologists physical status (I- II).
Patient with single renal stone size 2-3cm prepared for supine Percutaneous nephrolithotomy
Disqualifiers
Patient refusal.
Pregnancy
Morbid obese with Body mass index > 35 kg/m2.
Contraindication for spinal anesthesia.
Trial design
Parallel
Treatments tested in this trial
spinal anesthesia
Procedure/SurgerySpinal Anesthesia group: Patients included in this group will undergo supine Percutaneous nephrolithotomy under spinal anesthesia
General Anesthesia
Procedure/SurgeryGeneral Anesthesia : Patients included in this group will undergo supine Percutaneous nephrolithotomy under general anesthesia
Treatment groups
Trial outcomes
Primary outcomes
Patient satisfaction
Degree of patient satisfaction will be assessed according to a 5-point Likert scale (5: excellent, 4: Good, 3: Satisfactory, 2: Poor, 1: Very poor)
Secondary outcomes
Visual analog scale
Visual analog scale will be assessed after surgery over 24 hours using as (0 = no pain and 10 = intolerable pain).
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: