Skip to content

a clinical study to compare between two nerve blocks named Superior trunk block and Interscalene brachial plexus block for reducing pain in patients after open shoulder operations.

Comparison between Superior trunk block and Interscalene brachial plexus block for analgesia in open shoulder surgery: a pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/08/044997
Enrollment
40
Registered
2022-08-29
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: 8- Other Procedures

Interventions

Intervention1: Superior trunk block: a nerve block named Superior trunk block will be given Control Intervention1: Interscalene brachial plexus block: a nerve block named Interscalene brachial plexus

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I to III patients aged 18 to 70 years undergoing open shoulder surgeries which will include fracture proximal humerus, lateral end clavicle, AC joint or tuberosity fracture (Neerââ?¬•s classification of Proximal humerus fractures)

Exclusion criteria

Exclusion criteria: - Patient refusal to participate in the study - Patients with preexisting neuropathy affecting brachial plexus - Injury or infection at the block site - Allergy to one of the study medications

Design outcomes

Primary

MeasureTime frame
To compare the duration of analgesia between superior trunk block and interscalene block in patients undergoing open shoulder surgery Timepoint: To compare the duration of analgesia between superior trunk block and interscalene block in patients undergoing open shoulder surgery at 6 , 12 , 18 , and 24 hrs after block completion.

Secondary

MeasureTime frame
To compare between the two groups A. Incidence and severity of hemi-diaphragmatic paralysis B. Pain intensity on 10-point VAS (visual analogue scale) score at rest and movement (abduction of arm) post operatively in PACU, 6,12,18 and 24 hours after the block. C. Total analgesic consumption at 6,12, 18 and 24 hours post operatively. D. Time to return of normal sensation E. Patient satisfaction post operatively at 24 hours F. Complications like dyspnea, hiccups, hoarseness and Horner�s syndrome and neuropraxia within 24 hours postoperativelyTimepoint: post operatively in PACU, 6,12,18 and 24 hours after the block.

Countries

India

Contacts

Public ContactSourav D

AIIMS New Delhi

drchhavisawhney@gmail.com9818357051

Outcome results

None listed

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