Continuous Erector Spinae Block Versus Continuous Edge of Laminar Block on The Quality of Analgesia and Diaphragmatic Excursion in Patients With Multiple Rib Fractures

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-65
SponsorTanta University

About this trial

This prospective randomized clinical trial aims to compare the effect of continuous erector spinae plane block versus continuous edge of laminar block on the quality of analgesia and diaphragmatic excursion in patients with unilateral traumatic multiple rib fractures.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged between 21 and 65 years.

Both sexes.

With unilateral traumatic multiple fracture ribs (≥ 3), admitted to the surgical intensive care unit within the first day of trauma.

Disqualifiers

Patients' rejection.

Body mass index ≥ 35 (kg/m2).

Bleeding and Coagulation disorders.

Known hypersensitivity to the study drugs.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Erector spinae block

    Other intervention

    Patients will receive continuous ipsilateral erector spinae plane block.

  • Edge of lamina block

    Other intervention

    Patients will receive continuous ipsilateral edge of laminar block.

Treatment groups

70 Participants
are divided into 2 treatment groups
Group A: Erector spinae groupExperimental treatment 1 intervention
Group B: Edge of lamina groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Total morphine consumption

If the Numeric Rating Scale (NRS) is 4 or more IV morphine 3mg will be given.

Time frame
4 days postoperatively

Secondary outcomes

1

Degree of pain

The degree of pain will be assessed using the Numeric Rating Scale (NRS) at rest and on coughing will be assessed before the block, at 60 minutes after the block, and then every 8 hours for 4 days.

Time frame
4 days postoperatively
2

Diaphragmatic excursion

Diaphragmatic excursion will be assessed before the block, at 60 minutes after the block, and then every 8 hours for 4 days.

Time frame
4 days postoperatively
3

Incidence of adverse events

Incidence of adverse events such as hematoma, local anesthetic systemic toxicity, respiratory complications, pneumothorax, nausea, and vomiting.

Time frame
4 days postoperatively
4

Forced vital capacity

Forced vital capacity (FVC) will be assessed before the block, at 60 minutes after block, and then every 8 hours for 4 days.

Time frame
4 days postoperatively

Other outcomes

Sponsors and contacts

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