Serratus Posterior Plane Block vs Erector Spine Plane Block
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: new type of peripheral block Serratus Posterior Plane Block.
- Who it may be relevant to
- Registry conditions: Regional Anesthesia. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Czechia
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Continuous Serratus Posterior Plane Block Versus Continuous Erector Spine Plane Block for Video-assisted Thoracoscopic Surgery: a Prospective Randomized Non-inferiority Trial
Overview
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.
Interventions
- Procedure new type of peripheral block Serratus Posterior Plane Block
Intervention will be Serratus Posterior Plane Block.
Primary outcome measures
- Cumulative opioid dose in 72 hours [Time frame: from end of surgery to 72 hours after the end surgery]
Eligibility criteria
Inclusion criteria
- Patiens undergoing VATS-surgery
Exclusion criteria
- 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)
- Patient's refusal
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Czechia · 1 center
- Krajská zdravotní, a.s. - Masarykova nemocnice v Ústí nad Labem, o.z. — Ústí nad Labem
Identifiers
NCT: NCT07021131 · SERRATUS