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Post operative pain management in shoulder surgeries

A comparitive study of effect of suprascapular nerve block for postoperative analgesia in shoulder surgeries under general anesthesia using ropivacaine versus ropivacaine with nalbuphine as an adjuvant - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/102835
Enrollment
60
Registered
2026-02-03
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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: Supascapular nerve block using 8 mL of Ropivacaine (0.25%) + Nalbuphine 10 mg(1ml): 8 mL Ropivacaine 0.25% + Nalbuphine 10 mg (1 mL) used to administer suprascapular nerve block as a si

Sponsors

MGM MEDICAL COLLEGE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of ASA physical grade I , II , III Patients undergoing Shoulder Surgery under GA

Exclusion criteria

Exclusion criteria: History of infection at site of block Coagulopathies Patients with known hypersensitivity to Local anaesthetic or Nalbuphine Pregnant women Pre-existing peripheral neuropathy

Design outcomes

Primary

MeasureTime frame
Duration of postoperative analgesia, defined as the time interval (in minutes) from administration of ultrasound-guided suprascapular nerve block to the first request for rescue analgesia by the patient, assessed within the first 24 hours postoperatively.Timepoint: Within 24 hours postoperatively

Secondary

MeasureTime frame
Postoperative pain intensity assessed using the Numerical Rating Scale (NRS) at 1, 2, 4, 6, 12 & 24 hours after surgery. Total rescue analgesic requirement, including the number of doses & timing of rescue analgesia required within the first 24 hours postoperatively. Hemodynamic parameters, including heart rate & mean arterial pressure, recorded intraoperatively & postoperatively at predefined time intervals. Incidence of adverse effects, such as nausea, vomiting, pruritus, sedation & respiratory depression, observed within the first 24 hours postoperatively.Timepoint: Postoperative pain intensity 1, 2, 4, 6, 12 & 24 hours postoperatively Rescue analgesic requirement Within 24 hours postoperatively Hemodynamic parameters Intraoperatively & within 24 hours postoperatively Adverse effects Within 24 hours postoperatively

Countries

India

Contacts

Public ContactAmol Pandav

MGM MEDICAL COLLEGE AND HOSPITAL

amolpandav05@gmail.com9420249112

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026