FindTrial
Sign In

To study efficacy Of ultrasound guided erector spinae block for postoperative analgesia in laparoscopic cholecystectomy

To Study efficacy Of ultrasound Guided Erector Spinae Block For Postoperative Analgesia In Laproscopic Cholecystectomy.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/02/031218
Enrollment
40
Registered
2021-02-11
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: Ultrasound guided erector spinae block for post operative analgesia in laparoscopic cholecystectomy: After laparoscopic cholecystectomy patients will receive 40 ml of 0.25% bupivacaine

Sponsors

Saroj Kumar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)ASA 1 and 2. 2)Consenting Patients

Exclusion criteria

Exclusion criteria: 1)Age less than 18 and more than 65. 2)Non consenting Patients. 3)Bleeding Diathesis. 4)Pregnancy and Lactation. 5)Local skin infection.

Design outcomes

Primary

MeasureTime frame
opioids consumption by patients in post operative period.Timepoint: opioids consumption by patients in post operative period for 24 hrs—

Secondary

MeasureTime frame
Post operative pain score.Timepoint: 24 hours—

Countries

India

Contacts

Public ContactDr Swati

IGIMS , Patna

deepakswat@yahoo.com8544413241

Outcome results

None listed

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