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Clinical Trials/CTRI/2024/04/065274
CTRI/2024/04/065274Not yet recruitingPhase 3

Analyzing the efficacy of chest block in comparison with intravenous analgesia for acute pain management in closed chest trauma with a Numeric rating scale (NRS) score of 7 or more, presenting to the Emergency department - A Prospective Pragmatic Interventional study.

Christian Medical College Internal Fluid Research Grant1 site in 1 country70 target enrollmentStarted: May 1, 2024Last updated:

Trial Snapshot

Phase
Phase 3
Status
Not yet recruiting
Sponsor
Enrollment
70
Locations
1
Primary Endpoint
Reduction in pain score

Study Overview

Brief Summary

Patients who present to the emergency department (ED) with blunt thoracic trauma are usually managed  with intravenous analgesia including NSAIDS and opioids. Rib fractures are extremely painful and can lead to poor respiratory effort and hypoxia from thoracic splinting. Opioid and non-opioid analgesia often do not provide sufficient or consistent analgesia and may require doses where the adverse effects are more compared to the benefits especially in the elderly population or those with comorbidities such as obesity or reactive airway disease. Many patients in our ED receive a chest block which seems to provide sufficient and long lasting analgesia. Since the blocks are administered by only a few trained personnel in the department presently, many patients do not receive the blocks. In our study we wish to compare the analgesia and improvement in respiratory function between patients who receive a block and those who receive the standard analgesic management.. The analgesia achieved will be objectively scored by the numerical rating scale or visual analogue scale. Improvement in the respiratory function will be assessed with the change in tidal volumes on incentive spirometry. We will also look at success rates of performing these blocks in the emergency department setting by consultants trained to administer the blocks, as well as the average duration of action of the block.

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
18.00 Year(s) to 99.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • All adult patients with blunt thoracic traumas with 2 or more radiologically confirmed rib fractures.

Exclusion Criteria

  • Patient does not give consent.
  • Open chest wounds.
  • Polytraumatised patients
  • Patients who are haemodynamically unstable or require ICU care
  • Allergy or contraindications to NSAIDs/Paracetamol/Local anaesthetics
  • Pregnant women.

Outcomes

Primary Outcomes

Reduction in pain score

Time Frame: Reduction in pain score from 7 to less than 4, or by more than 50% from time of patient admission in the emergency department till discharge from emergency department, or till 12 hours in the ward.

Secondary Outcomes

  • 1.Success rate of the block in reducing the pain score(2.Compraison of patient satisfaction.)

Investigators

Sponsor
Christian Medical College Internal Fluid Research Grant
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Gokul Prakash

Christian Medical College and Hospital

Study Sites (1)

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