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Efficacy and safety of spinal anaesthesia for kidney stone surgeries

Clinical efficacy and safety of intrathecal anaesthesia for percutaneous nephrolithotomy - A prospective observational study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/063036
Enrollment
100
Registered
2024-02-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Spinal Anaesthesia: We will be checking for the clinical efficacy and safety of spinal anaesthesia in patients undergoing Percutaneous nephrolithotomy surgery. For this we will perform

Sponsors

Sri Venkateswara Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All adult patients above 18 years scheduled for elective PCNL

Exclusion criteria

Exclusion criteria: Patients who are not willing to participate in the study. Patients with general contraindications to Spinal anesthesia. Patients with known allergies to Spinal anesthesia drugs. Pregnant women and lactating mothers

Design outcomes

Primary

MeasureTime frame
Intraoperative hemodynamic stability will be assessed by observing the number of episodes of hypotension (systolic blood pressure below 90 mmhg), hypertension (systolic blood pressure more than 20% from baseline), bradycardia (absolute decrease in heart rate below 60 beats per minute) and tachycardia (heart rate more than 100 beats per minute).Timepoint: At baseline, during the procedure, before shifting to recovery room

Secondary

MeasureTime frame
(1) To find out conversion rate to general anaesthesia or supplementation to spinal anaesthesia (2) To find out patient discomfort at the end of surgery (before making the patient supine from prone position) on a likert type scale for discomfort (3)To find out patient satisfaction at follow up on 1st post operative day on a likert type scale for satisfaction (4) To find out occurrence of injury to lung & pleuraTimepoint: (1) During the procedure (2) At the end of procedure (3) Post operative day one (4) During procedure & post operatively

Countries

India

Contacts

Public ContactDr Uday Suraj

Sri Venkateswara Institute of Medical Sciences

aloksvims@gmail.com9493547653

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026