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Comparison of patient satisfaction with thoracic segmental spinal anaesthesia vs general anaesthesia for gynecomastia surgeries.

Comparison of patient satisfaction with thoracic segmental spinal anaesthesia with modified tumescent solution vs general anaesthesia with standard tumescent solution for liporeduction of gynecomastia: A Randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087847
Enrollment
50
Registered
2025-05-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: M799- Soft tissue disorder, unspecified

Interventions

Intervention1: Thoracic segmental spinal anaesthesia with modified tumescent solution: Spinal anaesthesia will be given with 5mg of isobaric levobupivacaine plus 25mcg fentanyl. Modified tumescent so

Sponsors

Dr. Sandeep Garee
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients coming for gynecomastia surgeries. 2. ASA 1-2

Exclusion criteria

Exclusion criteria: 1. Allergy to local anaesthetics 2. Contraindications to spinal anesthesia 3. Cardiac abnormalities (Mitral and Aortic stenosis, CAD etc) 4. ASA 3,4 and 5 5. Patients refusal

Design outcomes

Primary

MeasureTime frame
1. To compare the patient satisfaction of using SSA vs GA in patients undergoing liporeduction for gynecomastia surgeries. 2. To study the time to first rescue analgesia between segmental spinal anaesthesia vs GA for liporeduction in gynecomastia surgeries. Timepoint: 4 hours , 8 hours , 12 hours and 24 hours after the intervention—

Secondary

MeasureTime frame
1. To assess & compare the surgeon satisfaction of using SSA vs GA in patients undergoing liporeduction for gynecomastia surgeriesTimepoint: Immediately after the surgery;2. To compare the incidence of PONV among both the groupsTimepoint: 24 hours;3. To compare the incidence of hemodynamic variations among the groupsTimepoint: Every 5 min until end of Surgery & then every 15 min for next 3 hours.—

Countries

India

Contacts

Public ContactDr Sandeep Garee

All India Institute of Medical Sciences (AIIMS) Bibinagar

drsandeep189@gmail.com9989421851

Outcome results

None listed

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