Pain relief in thoracoscopic procedures without loss of consciousness

Efficacy of combined Thoracic Segmental Spinal Anaesthesia and Erector Spinae Plane Block in patients undergoing thoracoscopic procedures a prospective observational study - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/08/071781

Enrollment

Registered

2024-08-01

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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

Conditions

Health Condition 1: J869- Pyothorax without fistula

Interventions

Intervention1: Thoracic segmental spinal plus erector spinae plane block: Patients will receive thoracic segmental spinal at T5-T6 level with 1 ml of 0.5% isobaric levobupivacaine + 25 mcg fentanyl .

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA 1, 2 and 3 patients of either sex 2. Patients aged between 20 to 60 years 3. Patients undergoing thoracoscopic procedure

Exclusion criteria

Exclusion criteria: 1. Patient’s refusal 2. ASA 4 patients 3. Patients with known hypersensitivity to local anaesthetics 4. Patients with bleeding disorder 5. Patients with epilepsy 6. Mentally unstable patients 7. Patients with neurological deficits 8. Infection at local site

Design outcomes

Primary

Measure	Time frame
To investigate the analgesic efficacy of combined thoracic segmental spinal anaesthesia and erector spinae plane block in patients undergoing thoracoscopic proceduresTimepoint: 1,3,5,10,15,30,45,60,90 minutes	—

Secondary

Measure	Time frame
Sensory blockade level Changes in hemodynamic parameters intra-operatively SPO2 Heart rate Blood pressure Patient recovery and satisfaction Post-operative complications if anyTimepoint: Intraoperatively, 1,2,4,6,8,12,24 hours	—

Countries

India

Contacts

Public ContactDr Shwetha AH

Rajarajeswari Medical College and Hospital

ahshwetha@gmail.com09449795180

Outcome results

None listed

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