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To evaluates the safety and efficacy of spinal anaesthesia, peripheral nerve block, and monitored anaesthesia care for day care varicose vein surgery

Comparison of efficacy and safety profile of spinal anaesthesia, peripheral nerve block and monitored anaesthesia care for day care varicose vein surgery: A prospective randomized controlled study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/096420
Enrollment
99
Registered
2025-10-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: I838- Varicose veins of lower extremities with other complications

Interventions

Intervention1: To compare the efficacy of the spinal anaesthesia, peripheral nerve block and monitored anaesthesia care in term of Surgeons satisfaction using Likert scale: To compare the efficacy of

Sponsors

Operation Theater King George Medical University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients scheduled for saphenous varicose vein surgery. Age between 18 and 70 years. ASA I - II Written Informed consent will be taken.

Exclusion criteria

Exclusion criteria: Patient Refusal Known allergy to components of the anesthesia drugs. History of coagulopathy or bleeding disorders. History of drug abuse or chronic sedative use High cardiovascular risk Significant pulmonary disease

Design outcomes

Primary

MeasureTime frame
Efficacy: Postoperative pain scores (VAS/NRS) at different time intervals, time to first analgesic request, duration of analgesia. Safety: Incidence of anesthesia-related complications (hypotension, bradycardia, respiratory depression), postoperative nausea and vomiting (PONV), need for unplanned hospital admission.Timepoint: 2 to 24hrs—

Secondary

MeasureTime frame
Recovery parameters: Time to ambulation, discharge readiness, patient satisfaction scores. Adverse events: Incidence of deep vein thrombosis (DVT), surgical site infection, anaphylaxis. Analgesic requirement: Total opioid consumption in 24 hours post-surgery.Timepoint: 2 to 24 hrs—

Countries

India

Contacts

Public ContactProf Rajni Gupta

King Georges Medical University Lucknow

rgkgmu@gmail.com9839288980

Outcome results

None listed

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