Serratus Posterior Plane Block vs Erector Spine Plane Block

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMasarykova Nemocnice v Usti nad Labem, Krajska Zdravotni a.s.

About this trial

Analgesia related to the administration of local anesthetic solution into the fascia of erector spinae muscle is mediated by the effect of local anesthetic on the posterior and lateral branches of the anterior part of the spinal nerve. Comparable analgesic efficiency after the administration of both nerve blocks would reject the widespread theory of the paravertebral site of effect of the local anesthetic in ESPB.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patiens undergoing VATS-surgery

Disqualifiers

Age < 20 years

Body Mass Index >35 kg/m2

Technical difficulties with the nerve block administration and/or subsequent bolus application

Abnormal course of the surgery (e.g. conversion to thoracotomy) or the postoperative phase (e.g. surgical revision of the chest)

Trial design

Design model

Parallel

Treatments tested in this trial

  • new type of peripheral block Serratus Posterior Plane Block

    Procedure/Surgery

    Intervention will be Serratus Posterior Plane Block.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Erector spinae plane blockNo intervention 0 interventions
Group B: Serratus Posterior Plane BlockExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Cumulative opioid dose in 72 hours

Irrespective of the type of the block, 20 mls of 0.25 % bupivacaine will be administered to the block catether every 8 hours. Every patients will receive non-opioid analgesics according to standardized ward guideline. VAS score is recorded at least every 3 hours (except for time patient is asleep). Any time patient reports VAS score \>=5, he/she will receive 5 mg of morphine intravenously (or equivalent dose of Oxycodone per os). Cumulative dose of opioids will be recorded.

Time frame
from end of surgery to 72 hours after the end surgery

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: