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Analgesic effect of two nerve block techniques in patients with chest injury

Analgesic efficacy of ultrasound-guided erector spinae plane block versus costotransverse foramen block in patients with chest trauma presenting to emergency department: A randomized double-blind trial - NIL

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056163
Enrollment
58
Registered
2023-08-04
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: S299- Unspecified injury of thorax

Interventions

Intervention1: Costotransverse foramen block (CTFB): The level of CTFB will be decided as per the site of injury. The level of thoracic transverse process will be identified based on anatomical landma

Sponsors

Dr Chitta Ranjan Mohanty
Lead Sponsor
Department of Trauma and Emergency
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: I. All patients >=18 years of age of either gender with chest trauma and pain with a pain score of NRS >=5 at presentation. II. Patient presents within 72 hours of injury. III. Patients who are willing to give informed written consent.

Exclusion criteria

Exclusion criteria: I. Any infection at the proposed site of injection. II. Significant subcutaneous emphysema which obscures sonographic visualization of underlying anatomical structures. III. Patients who have known allergies to local anesthetic agents IV. Any painful distracting injury. V. Patients with known coagulopathy VI. Significant hypotension/shock (SBP

Design outcomes

Primary

MeasureTime frame
The primary outcome measure will be pain reduction on intervention in terms of Numerical rating scale (NRS) score after performing the ESPB or CTFB blockTimepoint: 20 minutes after performing the block.

Secondary

MeasureTime frame
The secondary outcome measure will be the time of onset & duration of analgesia as well as the success rate of block in either group.Timepoint: 10 minutes,20 minutes, 60 minutes & at the time of disposition of the patient from the emergency department

Countries

India

Contacts

Public ContactDr Aditya Vikram Prusty

All India Institute of Medical Sciences Bhubaneswar

drchitta8@gmail.com8280458275

Outcome results

None listed

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