Health Condition 1: F640- Transsexualism
Conditions
Interventions
Intervention1: Ultrasound-guided bilateral Erector Spinae Plane Block (ESB)
: Participants will be randomized into two groups after induction of standardized general anesthesia. The ESB group will rec
Sponsors
NIL
Eligibility
Inclusion criteria
Inclusion criteria: 1. Transgender males post-orchidectomy on estrogen therapy 2. Age 18-60 years 3. ASA PS I-III
Exclusion criteria
Exclusion criteria: 1. Those with significant liver or renal dysfunction 2. COPD, bronchial asthma 3. Allergy to ropivacaine 4. Local infection 5. On antidepressants or anxiolytics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of postoperative analgesiaTimepoint: post operative day 1(first 24 hours) | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes include postoperative VAS pain scores, intraoperative fentanyl requirement, total postoperative rescue analgesic consumption, intraoperative sevoflurane consumption, and incidence of adverse events such as postoperative nausea and vomiting (PONV), pneumothorax, and local anesthetic systemic toxicity.Timepoint: Postoperative pain scores will be assessed using the Visual Analogue Scale (VAS) at 0, 2, 4, 6, 12, and 24 hours after surgery. Intraoperative variables including fentanyl and sevoflurane consumption will be recorded during surgery. Rescue analgesic requirement and adverse events will be monitored during the first 24 postoperative hours, and patients will be followed up on postoperative day one. | — |
Countries
India
Contacts
Public Contactaishwarya prasad
Amrita institute of medical sciences
Outcome results
None listed