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To Compare hemodynamic parameters during Combined spinal epidural anaesthesia with General anaesthesia in patients undergoing Percutaneous Nephrolithotomy

A Randomized control trial to compare hemodynamic parameters of patients undergoing Percutaneous Nephrolithotomy under Combined spinal-epidural and General anaesthesia in a tertiary hospital. - CSEGAPCNL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/032655
Enrollment
90
Registered
2021-04-08
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: N200- Calculus of kidney

Interventions

Intervention1: Combined Spinal Epidural anaesthesia for Percutaneous Nephrolithotomy: Combined Spinal epidural anaesthesia has some advantage over General Anaesthesia, such as lower postoperative pain

Sponsors

SRM IST
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients between 18-65 years with physical status I or II of American Society of Anesthesiologists (ASA) undergoing PCNL

Exclusion criteria

Exclusion criteria: All patients with spinal deformity Local infection at injection site History of any neuromuscular or psychiatric disorder or chronic pain Hypertension, diabetes and coagulation disorders Patients with hypersensitivity to local anaesthetics, substance abusers. Patients with solitary kidney Patients posted for bilateral PCNL

Design outcomes

Primary

MeasureTime frame
Primary objective is to compare Pulse rate, Mean arterial pressure in patients undergoing percutaneous nephrolithotomyTimepoint: 4 hours—

Secondary

MeasureTime frame
Secondary aim is to compare blood loss, duration of postoperative analgesia in patients undergoing percutaneous nephrolithotomy. Timepoint: 4 hours—

Countries

India

Contacts

Public ContactKsheerabdhi S

SRM Medical College Hospital and Research Centre

dranand@outlook.com9865282288

Outcome results

None listed

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