Actively Recruiting

Phase 3
Age: 18Years +
All Genders
NCT03984656

Evaluation of the Analgesia by Serratus Plane Block During Pleural Drainage in Intensive Care Unit.

Led by Centre Hospitalier Universitaire, Amiens · Updated on 2026-05-13

70

Participants Needed

1

Research Sites

378 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Pleural drainage under local anesthesia is a frequent practice in resuscitation, experienced as an unpleasant and painful event for patients. Pain management is an important issue for early rehabilitation, decrease hospitalisation's cost and shortening the length of stay in intensive care unit (ICU). A new type of locoregional anesthesia called Serratus plane block described by Blanco in 2013 showed a benefit in per and postoperative analgesia in thoracic surgery and carcinologic breast surgery, allowing a decrease in morphine use and an improvement of the patient's general satisfaction. Serratus plane block is a very effective technique in chest wall analgesia, easy and safe to perform, with few complications. No studies to date have evaluated this anesthetic practice in intensive care for pleural drainage. This technique could be used outside the operating room to improve the intensive care patients, who often have heavier pathologies and greater pain, such as patients with chest trauma or patients with cardiac or respiratory disease. The investigators would like to conduct a preliminary study of superiority in the CHU Amiens intensive care unit, to study the interest of the Serratus plane block in comparison with local anesthesia on the management of acute pain during pleural drainage.

CONDITIONS

Official Title

Evaluation of the Analgesia by Serratus Plane Block During Pleural Drainage in Intensive Care Unit.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients over 18 years old
  • Non-intubated patient with spontaneous breathing
  • Patient provides free and informed consent
  • Affiliated with a social security scheme
  • Hospitalized in ICU, including surgical, cardiothoracic, respiratory ICU or continuous care unit
  • Requires pleural drainage of gas or fluid
  • Conscious and not sedated
Not Eligible

You will not qualify if you...

  • Under 18 years old
  • Patient refusal to participate
  • Under legal guardianship or deprived of liberty
  • Pregnant, parturient, or breastfeeding women
  • Contraindication to lidocaine or ropivacaine
  • Coagulation disorders

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHU Amiens

Amiens, France, 80000

Actively Recruiting

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Research Team

L

Louise Badoux, MD

CONTACT

L

Louise Badoux, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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