To compare erector spinae plane block and subcostal transverse abdominis plane block for post operative pain after laparoscopic cholecystectomy

Comparison of erector spinae plane block and subcostal transverse abdominis plane block for post operative analgesia after laparoscopic cholecystectomy - Nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2024/10/074543

Enrollment

Registered

2024-10-01

Start date

Unknown

Completion date

Unknown

Last updated

2024-10-14

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

Conditions

Health Condition 1: K803- Calculus of bile duct with cholangitis Health Condition 2: K804- Calculus of bile duct with cholecystitis Health Condition 3: K805- Calculus of bile duct without cholangitis or cholecystitis Health Condition 4: K806- Calculus of gallbladder and bile duct with cholecystitis Health Condition 5: K807- Calculus of gallbladder and bile duct without cholecystitis Health Condition 6: K800- Calculus of gallbladder with acutecholecystitis Health Condition 7: K801- Calculus of ga

Interventions

Intervention1: ERECTOR SPINAE PLANE BLOCK: Bilateral ultrasound guided erector spinae plane block with 20ml of 0.2 percent ropivacaine on each side maximum 250 mg after the induction of general anaest

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients scheduled for laparoscopic cholecystectomy. 2.American Society of Anaesthesiologist ASA I-II 3.Patient’s cognitive ability to comprehend visual analogue scale (VAS)

Exclusion criteria

Exclusion criteria: 1.Patients allergic to local anaesthetics being used 2.Infection at the site of infiltration of local anaesthetic 3.Patients with uncontrolled bleeding diathesis evidenced by history and laboratory investigations 4.Patients unable to comprehend VAS score 5.Patients with history of chronic opioid abuse 6.BMI more than 35 7.Refusal to participate in the study

Design outcomes

Primary

Measure	Time frame
The time to demand for first rescue analgesic in patients in both groups undergoing laparoscopic cholecystectomy under general anaesthesia.Timepoint: at 0,2,4,6,12,20 and 24 hour	—

Secondary

Measure	Time frame
1.Consumption of total rescue analgesic (tramadol) in first 24 hours after surgery in both groups. 2.To compare effect on hemodynamic parameters Blood pressure , heart rate , respiratory rate, SpO2Timepoint: at 0,2,4,6,12,20 and 24 hour	—

Countries

India

Contacts

Public ContactDr Neeru Luthra

DAYANAND MEDICAL COLLEGE and HOSPITAL LUDHIANADayanand Medical College and Hospital, Ludhiana

drneeru1977@yahoo.co.in9815500960

Outcome results

None listed

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