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A clinical study to compare the paralysis of diaphragm after giving regional anesthesia for upper limb surgeries via different approaches

Comparison of Hemidiphragmatic paralysis in Supraclavicular versus Costoclavicular Block A Prospective Controlled Study - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065368
Enrollment
84
Registered
2024-04-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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: Costoclavicular Block using injection Ropivacaine: Dose : 30 ml of 0.5% concentration of injection Ropivacaine. Time of observation: After 30 minutes B-mode ultrasound examination of th

Sponsors

Dr Sayantanee Roy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18-60 years ASA 1 and 2 Scheduled for elective orthopaedic upper limb surgery under supraclavicular brachial plexus block and costoclavicular brachial plexus block Informed and written consent to participate in the study

Exclusion criteria

Exclusion criteria: Patients with known hypersensitivity to local anaesthetic agent Infection at the site of block Patient with known respiratory disorder Patient whose pre operative SpO2 is less than 95% Patients with known coagulopathy or on anti-coagulation therapy Patients with diabetes mellitus Pregnant and lactating mother Morbid obesity Patients on chronic analgesic therapy Patients with peripheral vascular disease

Design outcomes

Primary

MeasureTime frame
1. To compare the incidence of hemi diaphragmatic paralysis with supraclavicular and costoclavicular brachial plexus approach Timepoint: Outcome will be assessed at 30 minutes after giving the block in the two groups .

Secondary

MeasureTime frame
1.To compare the extent of diaphragmatic excursion between both groups 2. To check for side effects and complications 3.To compare the onset of block between two groups 4.To compare the duration of analgesia between two groups. Timepoint: Outcome will be assessed at the following time intervals at rest : 0 hour , 3 minutes ,15 minutes ,30 minutes.

Countries

India

Contacts

Public ContactDr Sayantanee Roy

Guwahati Medical College and Hospital

faizaahmedtalukdar@gmail.com9864031429

Outcome results

None listed

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