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An observational study about the effect of COSTOCLAVICULAR NERVE BLOCK to provide surgical anesthesia and postoperative analgesia in upper limb surgeries

COSTOCLAVICULAR BLOCK FOR SURGICAL ANAESTHESIA IN HUMERUS FRACTURES: AN OBSERVATIONAL STUDY - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/05/087074
Enrollment
66
Registered
2025-05-19
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M849- Disorder of continuity of bone, unspecified

Interventions

Intervention1: Nil: Nil

Sponsors

PINGILI SAI NIKITHA
Lead Sponsor
DR BIJI K P
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients between age group of 18-65years 2.ASA- 1&2 3.Emergency and elective humerus and forearm surgeries 4.Weight =50-80kgs and height = 140-180cms

Exclusion criteria

Exclusion criteria: 1.Previous surgeries over infraclavicular fossa 2.Aberrant vascular anatomy in the cord clusters 3.Patient with coagulopathy or on anticoagulants 4.Infection at the site of injection 5.Allergy to local anaesthetic 6.Patients with neuromuscular disease or neurological deficits

Design outcomes

Primary

MeasureTime frame
1.To assess the costoclavicular block success rate 2.To assess the surgical successTimepoint: 4WEEKS—

Secondary

MeasureTime frame
1.To assess Block performance time Timepoint: 18months; 2.To assess Incidence of hemidiaphragmatic palsy at 30minutes after the block Timepoint: 18months;To assess Block performance time 3.To assess Postoperative analgesia Timepoint: 18months; 4.To assess Incidence of adverse events Timepoint: 18months—

Countries

India

Contacts

Public ContactPINGILI SAI NIKITHA

GOVERNMENT MEDICAL COLLEGE KOZHIKODE

drbijikp@gmail.com9895131600

Outcome results

None listed

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