Novel use of Erector spinae block during laparoscopic surgeries

Efficacy of erector spinal block during laparoscopic surgeries

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/09/036754

Enrollment

Registered

2021-09-22

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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: Efficacy of erector spinal block during laparoscopic surgeries: 25 patients will be given ultrasound guided erector spinae block using 0.25% bupivacaine 20ml bilaterally at T5 Spinous p

Eligibility

Inclusion criteria

Inclusion criteria: Asa grade 1 and 2 Patients undergoing laparoscopic surgeries under general anaesthesia Haemodynamically stable patients with all routine investigations within normal limits without comorbidities Patients not on any cardiac related drugs

Exclusion criteria

Exclusion criteria: Asa 3 or more Patients posted for emergency procedure Major neurological,cardiac,respiratory,metabolic,renal,hepatic diseases with coagulation abnormalities Cardiac comorbidities Patients refusal

Design outcomes

Primary

Measure	Time frame
To determine the effectiveness of erector spinae block for haemodynamic stability during laparoscopic surgeriesTimepoint: Heart rate, systolic and diastolic blood pressure will be monitored at baseline, at induction of pneumoperitoneum, and every 10 mins thereafter untill the completion of surgery	—

Secondary

Measure	Time frame
The amount of Fentanyl required intraoperatively and the amount of inhalational agent required intraoperatively will be measured.Timepoint: The amount of fentanyl required intraoperatively, given in aliquots whenever heart rate or blood pressure increases 20% above the baseline values will be recorded for the duration of surgery. The amount of inhalational agent (Isoflurane) used intraoperatively during the period of surgery will be measured.	—

Measure

Time frame

The amount of Fentanyl required intraoperatively and the amount of inhalational agent required intraoperatively will be measured.Timepoint: The amount of fentanyl required intraoperatively, given in aliquots whenever heart rate or blood pressure increases 20% above the baseline values will be recorded for the duration of surgery. The amount of inhalational agent (Isoflurane) used intraoperatively during the period of surgery will be measured.

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Countries

India

Contacts

Public ContactSumedha Biswas

Dr.D.Y. Patil medical college,hospital and research centre

biswasumedha@gmail.com9094042623

Outcome results

None listed

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