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Study of comparison of different modes of analgesia for upper abdominal surgery

Comparison of intrathecal morphine with thoracic epidural and erector spinae plane block for quality of recovery in upper abdominal surgery: A prospective, triple-arm, open label randomized study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052219
Enrollment
120
Registered
2023-05-02
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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: intrathecal morphine: patients will receive intrathecal morphine at L 3-4, or 4-5 intervertebral space in the dose of 4 mcg/kg (upto a maximum dose of 300 mcg, through a single dilution

Sponsors

Swati Singh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patient posted for upper abdominal surgery 2 Patients of ASA physical status 1, 2 & 3

Exclusion criteria

Exclusion criteria: 1 Patient’s refusal to participate 2 Patients of ASA physical status 4 3 Any allergy to local anaesthetics/ opioids 4 Coagulation disorders 5 Infection at the site of intervention 6 History of any underlying cardiac, renal dysfunction 7 Pregnant patient

Design outcomes

Primary

MeasureTime frame
Quality of recovery score (QoR)-15 scoreTimepoint: 24 hour postoperative—

Secondary

MeasureTime frame
1.Numerical Rating Scale (NRS) Score at 2,4,8,12,24 hrs post op 2.Postoperative complications in either groups 3.Hemodynamic parameters 4.Time to first rescue analgesia and total dose in first 24 hrs Timepoint: 2,4,8,12,24 hours—

Countries

India

Contacts

Public ContactDr Swati Singh

Indira Gandhi Institute of Medical Sciences, Patna

drswatisingh21@gmail.com9878309230

Outcome results

None listed

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