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Hemidiaphragmatic paralysis compared between supraclavicular and infraclavicular blocks

comparative evaluation of incidence of hemidiaphragmatic paralysis between supraclavicular and infraclavicular brachial plexus blockade.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/047720
Enrollment
52
Registered
2022-11-28
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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: GROUP A -SUPRACLAVICUKAR BLOCK: 0.5% Bupivacaine 20ml adminstered during supraclavicular block. duration 2hours Intervention2: GROUP -B INFRACLAVICULAR BLOCK: 0.5% Bupivacaine ,20ml ad

Sponsors

DRKRITHIKA U
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: RIGHT ELBOW AND BELOW ELBOW SURGERY AMERICAN SOCIETY OF ANESTHESIOLOGISTS PHYSICAL STATUS I to III ABLE TO GIVE INFORMED CONSENT BODY WEIGHT >50 KG

Exclusion criteria

Exclusion criteria: PATIENT REFUSAL KNOWN /SUSPECTED ALLERGY TO LOCAL ANESTHETICS PREGNANCY BODY MASS INDEX >35Kg/m2 OBSTRUCTIVE LUNG DISEASE SUSPECTED PHRENIC NERVE PALSY DIAPHRAMATIC DYSFUNCTION

Design outcomes

Primary

MeasureTime frame
To analyse the incidence of hemidiaphramatic paralysis between infraclavicular block and supraclavicular block with 20 ml of 0.5%Bupivacaine by measuring ultrasound guided diaphramatic excursion in m mode from the baseline to deep inspiration values recorded both pre block and post block(2hours ) and compared. Timepoint: To analyse the incidence of hemidiaphramatic paralysis seen in infraclavicular block and supraclavicular block Using same volume of local anesthetic drug before blockade in holding area baseline excursion value noted and after 2hours of block measuring diaphragmatic excursion value noted

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactUKrithika

Sri RamachandraInstitute of Higher Education and Research

reetharun@gmail.com9840529863

Outcome results

None listed

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