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Effect of a local block/injection on the quality of recovery after operation, using a questioner in laparoscopic Cholecystectomy surgeries

Effect of Erector spinae plane block on the Postoperative quality of recovery, using QoR-40 scale after laparoscopic Cholecystectomy- A randomized controlled clinical study - nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068995
Enrollment
66
Registered
2024-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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 Health Condition 2: 8- Other Procedures

Interventions

Intervention1: ESP Block under USG in Study group: I am comparing between two groups undergoing elective laparoscopic cholecystectomy, in which one group receives erector spinae plane block using inj

Sponsors

DR DN MEDICAL COLLEGE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of ASA grade 1 and 2 posted for elective laparoscopic cholecystectomy of duration less than 90 minutes.

Exclusion criteria

Exclusion criteria: patients refusal to participate, known case of allergic to the study drug, having pre-existing wound at the site of injection, a case of chronic pain syndrome, on prolonged opioid therapy, coagulopathy, patient with history of previous abdominal surgeries, and surgery exceeding more than 90 minutes.

Design outcomes

Primary

MeasureTime frame
to compare quality of recovery between group receiving Erector spinae plane block and control group during first 24 hours after Laparoscopic Cholecystectomy.Timepoint: to compare quality of recovery between group receiving Erector spinae plane block and control group during first 24 hours after Laparoscopic Cholecystectomy.

Secondary

MeasureTime frame
comparing between two groups The duration of Analgesia Cumulative dose of rescue analgesia & intra operative hemodynamic parameters.Timepoint: Duration of analgesia is when the patient requires Painkiller & intra operative parameters are recorded at a defined interval. Outcome assessment will be started at Baseline & 5 min 10min 15min 20min 30min 40min 60min & 90min. patient will be observed up to 24 hours post operatively for quality of recovery.

Countries

India

Contacts

Public ContactDr Chetan Chauhan

Dr.SN Medical college

chetanchauhan28@gmail.com8794760267

Outcome results

None listed

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