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compare effect of two nerve blocks for pain relief in shoulder manipulation

Comparison 0f Analgesic Efficacy of Interscalene Block And Peri-Capsular Nerve Group Block In Patients Undergoing Shoulder Manipulation Procedure: A Non-inferiority Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/057680
Enrollment
60
Registered
2023-09-15
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

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: Interscalene block (ISB): receive ISB nerve block with 15 ml of 0.5% ropivacaine with 1 in 2 lakh adrenaline. The block will given before start of shoulder manipulation and effect will

Sponsors

AIIMS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA I to III patients. 2. Age group of 18-70 years. 3. Scheduled for elective unilateral shoulder manipulation procedure.

Exclusion criteria

Exclusion criteria: 1.Patients who refused to participate in the study. 2. Patients with a history of cardiac, renal, or hepatic disease. 3.Patients with pre-existing neurologic deficits or neuropathy affecting the brachial plexus. 4. Patients with contraindications to peripheral nerve block. 5. Patients with known allergy to local anaesthetic drugs.

Design outcomes

Primary

MeasureTime frame
To compare total postoperative morphine consumption in 24hrs between patients undergoing ISB and PENG block around shoulder for shoulder manipulation surgeryTimepoint: 24hrs after block

Secondary

MeasureTime frame
• Successful completion of manipulation procedure •Ease of procedure on a Likert Scale of 0-2 •Visual analogue scale (VAS) score for pain ranging from 0 - 10 •Pre & post- block Diaphragmatic excursion •Incidence of motor block (0, 8, 24 hr) •Proportion of patients with moderate to severe pain (VAS more than 4) • Motor blockade after block (total/partial/absent) •Time for initiation of shoulder mobilisation •Degree of Shoulder abduction possible at 24 hrs • Patient satisfaction (0-10) at 24 hrs postoperatively ( vascular puncture, parasthesia, LA toxicity, hoarsness, PONV) Timepoint: time point 0,2,4, 8 and 24 hours after the procedure

Countries

India

Contacts

Public ContactAnju Gupta

AIIMS

dranjugupta2009@rediffmail.com9911573371

Outcome results

None listed

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