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Comparative Study Between Spinal Anesthesia Versus General Anesthesia in Supine Percutaneous Nephrolithotomy Operation

ConditionsSpinal AnesthesiaPercutaneous NephrolithotomyGeneral Anesthesia
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age22-65
SponsorTanta University

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • spinal anesthesia

    Procedure/Surgery

    Spinal Anesthesia group: Patients included in this group will undergo supine Percutaneous nephrolithotomy under spinal anesthesia

  • General Anesthesia

    Procedure/Surgery

    General Anesthesia : Patients included in this group will undergo supine Percutaneous nephrolithotomy under general anesthesia

Treatment groups

70 Participants
are divided into 2 treatment groups
Group A: Spinal AnesthesiaExperimental treatment 1 intervention
Group B: General AnesthesiaExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

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)

Time frame
24 hours

Secondary outcomes

1

Visual analog scale

Visual analog scale will be assessed after surgery over 24 hours using as (0 = no pain and 10 = intolerable pain).

Time frame
24 hours

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Tanta University

Lead sponsor

Source ClinicalTrials.gov

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