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A Clinical trial to compare the effect USG guided single injection Erector Spinae Plane Block and Serratus Anterior Plane Block for postoperative analgesia in thoracic surgery

Comparison of USG guided single injection Erector Spinae Plane Block versus Serratus Anterior Plane Block for postoperative analgesia in thoracic surgery A Randomised Control Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/073154
Enrollment
60
Registered
2024-08-30
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: USG Guided ESP Block and SAP Block in Thoracic Surgeries: Comparison Between USG Guided ESP Block and SAP Block for postoperative analgesia in Thoracic Surgeries Control Intervention1:

Sponsors

DR SN Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria:  Adult patients, aged between 18 to 45 years and undergoing elective Thoracic surgeries under general anesthesia who belongs to ASA PSI, II

Exclusion criteria

Exclusion criteria: 1.Patients with BMI more than 30 kg/m2 or BMI less than 18 kg/m2 2.Patient refusal 3.Age less than 18 years old 4.Pregnant woman 5.History of any allergy to related perioperative medications 6.Previous lumbar spine surgery 7.Existing contraindications to nerve block such as coagulopathy, local and systemic infections 8.Those patients who are intubated for more than 4 hours postoperatively and shifted to postoperative ward will be excluded from the study 9. Patients who experience block failure 10.Those patients complaining of pain within 2 hours of postoperative period will be considered as block failure and are excluded from the study

Design outcomes

Primary

MeasureTime frame
The primary objective to compare SAPB or ESPB for postoperative analgesia following thoracic surgery, as determined by the time until the first analgesic requirement in the postoperative periodTimepoint: The primary objective to compare SAPB or ESPB for postoperative analgesia following thoracic surgery, as determined by the time until the first analgesic requirement in the first 24 hours postoperative period

Secondary

MeasureTime frame
1.VAS score at rest and while coughing at 2, 4, 8, 24, 48 hours postoperatively 2.Consumption of injection tramadol in first 24 hours of postoperative period 3.Hemodynamic parameters 4.Block related complications hematoma, pneumothorax, nerve injury till a period of 2 weeks 5.Length of Hospital stayTimepoint: 1.VAS will be recorded after the extubation, and at interval of 10 min thereafter till 60 mins to confirm the time of onset analgesia, then interval of hourly upto 4 hours followed by every 4 hours up to 24 hours post-operative 2.Hemodynamic parameters will be monitored after extubation and at the interval of 10min thereafter till 60 mins, then hourly upto 4 hours followed by 4 hourly upto 24 hours postoperatively

Countries

India

Contacts

Public ContactDr Rakesh Karnawat

DR SN Medical College

dr.rakeshkarnawat@yahoo.com9828033321

Outcome results

None listed

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