Post operative analgesic consumption with or without sono-guided Erector Spinae Plane Block in patients undergoing abdominal surgery: A randomised, controlled, interventional study.

Post operative analgesic requirement with or without sono-guided erector spinae plane block in patients undergoing abdominal surgery: A randomized, controlled interventional study, SMS Hospital, Jaipur

Status

Active, not recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/02/030907

Enrollment

Registered

2021-02-01

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: K806- Calculus of gallbladder and bile duct with cholecystitis Health Condition 2: K432- Incisional hernia without obstruction or gangrene Health Condition 3: C23- Malignant neoplasm of gallbladder Health Condition 4: C250- Malignant neoplasm of head of pancreas Health Condition 5: K689- Other disorders of retroperitoneum Health Condition 6: K638- Other specified diseases of intestine Health Condition 7: K318- Other specified diseases of stomach and duodenum Health Condition

Interventions

Intervention1: Erector Spinae Plane Block: Erector Spinae Plane Block under ultrasound guidance using 25ml of 0.25% ropivacaine. Control Intervention1: Control Group: Patients undergoing abdominal sur

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients belonging to American Society of Anesthesiologists (ASA): Grade I: Without co-morbid conditions Grade II: Controlled co-morbid conditions Grade III : Poorly controlled co-morbid conditions 2.Weight 40-80 kg

Exclusion criteria

Exclusion criteria: 1.Patients not willing to participate in the study 2.H/O allergic reactions to local anesthetics 3.Patients on anticoagulant therapy and H/O coagulation disorders 4.Local infection at the proposed site of puncture for Erector Spinae Plane block 5.Chronic use of opioids or corticosteroids.

Design outcomes

Primary

Measure	Time frame
To determine the difference in mean analgesic dose required post operative period in both groupsTimepoint: 12 hours and 24 hours	—

Secondary

Measure	Time frame
To determine the time of first rescue analgesic in both groups.Timepoint: 12 hours , and every 1 hour thereafter upto 24 hours.	—

Countries

India

Contacts

Public ContactDr Sushil K Bhati

Sawai Man Singh Medical College

drsushilbhati@yahoo.co.in9414779786

Outcome results

None listed

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