FindTrial
Sign In

Comparision of satisfaction of people who undergoing ureterorenoscopic lithotripsy surgery with different anaesthetic techniques

Comparing patient satisfaction with general anaesthesia and regional anaesthesia in ureterorenoscopic lithotripsy surgery: A cross - sectional,prospective, observational clinical comparative study - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/04/085355
Enrollment
200
Registered
2025-04-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: N00-N99- Diseases of the genitourinary system

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Sri Ramachandra medical College and research hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - physical status of American society of anaesthesiologists (ASA) grade 1,2,3 - staying in hospital for more than 24 hours postoperatively

Exclusion criteria

Exclusion criteria: -patients on antiplatelet or anticoagulant drugs -patients admitted in intensive care units -patients having local infection at site of injection -patients with bleeding coagulopathy, delirium, confusion - uncooperative patients - Emergency surgeries

Design outcomes

Primary

MeasureTime frame
Patient satisfaction between two groups as per predesigned peripoerative questionnaireTimepoint: First 24 hours—

Secondary

MeasureTime frame
Post operative Visual Analogue ScoreTimepoint: Pain at 2 hours, 12 hours, 24 hours;Duration of analgesia( time to first request dose analgesia IV Paracetamol 10-15mg/kg )Timepoint: Nil;The length of hospital stay was calculated in days from the day of surgery till day of dischargeTimepoint: Nil—

Countries

India

Contacts

Public ContactDrArul Murugan

Sri Ramachandra institute of higher education and research

rampond@gmail.com9380537411

Outcome results

None listed

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