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Comparison of incidence of weakness of same side diaphragm following two different approaches of brachial plexus block.

Comparison of incidence of ipsilateral hemidiaphragmatic paresis following supraclavicular and costoclavicular approach to brachial plexus block. - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056564
Enrollment
50
Registered
2023-08-16
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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: Ultrasound guided supraclavicular brachial plexus block.: Patient will be administered ultrasound guided supraclavicular brachial plexus block for elective surgery below midarm. Inciden

Sponsors

Pt B D Sharma PGIMS Rohtak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients having American Society of Anesthesiologists (ASA) grade I-III, scheduled to undergo elective surgery below midarm of less than 2 hours duration, under regional anaesthesia.

Exclusion criteria

Exclusion criteria: Patients with -Significant pulmonary disease -History of psychiatric illness. -Diabetes mellitus, neuropathy, patients receiving opioids for chronic pain therapy -Known coagulopathy or on anticoagulant therapy. -Infection at the injection site. -Pregnant and lactating female patients. -Hypersensitivity to local anesthetic drug used. -Patient refusal and inability to give informed consent. will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
USG assessment of ipsilateral hemidiaphragmatic excursion.Timepoint: -Before performing supraclavicular/costoclavicular approach to brachial plexus block. - 30 min after performing supraclavicular/costoclavicular approach to brachial plexus block.—

Secondary

MeasureTime frame
Assessment of Motor blockTimepoint: -5 minutes after giving block -10 minutes after giving block -15 minutes after giving block -20 minutes after giving block -25 minutes after giving block -30 minutes after giving block;Assessment of sensory blockTimepoint: -5 minutes after giving block -10 minutes after giving block -15 minutes after giving block -20 minutes after giving block -25 minutes after giving block -30 minutes after giving block;Patient satisfaction using visual analogue scale (VAS)Timepoint: - Immediately after performing block - After the completion of surgery—

Countries

India

Contacts

Public ContactDr S Gowrishankar

PT.B.D.Sharma PGIMS Rohtak

dr.jatinlal@gmail.com9728265511

Outcome results

None listed

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