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Ultrasound guided infraclavicular brachial plexus block with 2 different approaches

An observational study of ultrasound guided infraclavicular brachial plexus block with Costoclavicular and Retroclavicular approaches for upperlimb orthopedic surgeries - Nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067845
Enrollment
60
Registered
2024-05-24
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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: Infraclavicular brachial plexus block: Patients posted for upper limb orthopaedic surgery and fulfilling my inclusion criteria Usg guided Infraclavicular brachial plexus block will be g
-Inj. Bupivacaine(0.5%) 20 ml ,Inj. Lignocaine (2%) 10 ml, Inj. Dexamethasone 2 ml. Total 32 ml volume will be given.I will observe the block performance time ,quality of block, will observe the Dura

Sponsors

Government medical college and new civil hospital Surat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients who will undergo planned upper limb surgeries under usg guided Infraclavicular brachial plexus block with Costoclavicular and Retroclavicular approaches and giving written informed consent. 2. Patients belonging to ASA class 1, 2,3 . 3.Patients of either sex, in the age group of 18 to 65yrs.

Exclusion criteria

Exclusion criteria: 1. Patients with known hypersensitivity to local anaesthetics. 2. Infection at the site of block . 3. Morbidly obese patient. 4.Patients with neurological, psychiatric or neurovascular disorders. 5.Patients with major cardio-pulmonary or hepato renal compromise. 6. Pregnant patients.

Design outcomes

Primary

MeasureTime frame
1) Block performance time. 2) Block characteristics- onset and duration of sensory and motor block 3)Quality of block.Timepoint: 1) Block performance time will be assessed from time of needle insertion to time of injecting drug 2) Block characteristics- onset and duration of sensory and motor block for 24 hours 3)Quality of block.

Secondary

MeasureTime frame
1)Duration of post operative analgesia and requirement of analgesics in 24 hours. 2)Intraoperative Hemodynamic changes. 3)Complications/Adverse events if anyTimepoint: Till 24 hours after giving block

Countries

India

Contacts

Public ContactDr Bansari N Kantharia

New surat civil hospital Surat

bansarikantharia@gmail.com9825690177

Outcome results

None listed

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