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Serratus Plane Block for Rib Fractures

Effect of the Serratus Plane Block on the Outcome in Patient With Multiple Rib Fractures: A Prospective, Randomized, Controlled Trial

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03664973
Enrollment
0
Registered
2018-09-11
Start date
2018-09-03
Completion date
2023-12-30
Last updated
2025-06-25

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

Conditions

Chest Trauma, Chest Pain

Brief summary

Patients with ipsilateral multiple rib fractures will be randomized to receive either a single-shot ultrasound-guided serratus plane block, or a continuous serratus plane block within 24h from the chest trauma. Primary outcome is the difference in forced respiratory volume (FEV1) at 72h.

Detailed description

Patients admitted in emergency department with a chest trauma and ipsilateral multiple rib fractures, will be randomized as described above. All patients will receive the serratus block with a ropivacaine 0.37% solution 20 ml. Then, they will randomized to receive either a peripheral catheter placed above the 5th rib on the middle axillary line, or nothing. In all patients postoperative analgesia also include Paracetamol 1g IV each 6h and a patient controlled analgesia (PCA) of morphine set out as follow: bolus 1 mg, loch out 15 min, max 4 boluses each hour. In all patients an arterial blood sample for gas analysis and a FEV1 will be achieved before the block, after 1 hour and at 72h.

Interventions

Local anesthetic infusion though a peripheral nerve catheter placed on the 5th rib under the serratus plane

Sponsors

Azienda USL Reggio Emilia - IRCCS
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* 2 o more ipsilateral rib fractures * Trauma within 24h from hospital admission * Informed consent

Exclusion criteria

* Chest drain * head trauma * bilateral rib fractures * Intensive care admission

Design outcomes

Primary

MeasureTime frameDescription
Pulmonary change functionday 0 and day 3FEV 1

Secondary

MeasureTime frameDescription
Numerical rating scale (NRS) of painday 0, day 1, day 2, day 3, day 4Pain both at rest and on movement on a 0-10 scale where 0 is the best and 10 the worst
Morphineday 0, day 1, day 2, day 3, day 4morphine requirement
hospital stayday 1, day 2, day 3, day 4, day 5, day 6, day7time to fill the discharge criteria

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026