Lung Cancer Clinical Trial

Efficacy Between Serratus Plane Block And Local Infiltration In Vats

Summary

Robotic video-assisted thoracoscopic surgery (VATS) is increasingly being used as it is a less invasive surgery compared to traditional methods, but the acute pain at an early stage after VATS has a major impact on perioperative outcomes. Effective post operative analgesia is believed to reduce morbidity, quicken recovery, improve patient outcome and reduce hospital costs. The site and extent of the incision influences the degree of pain due to disruption of intercostal nerves as well as inflammation of chest wall and pleura. Neuraxial and systemic opioids have been a gold standard as a part of multimodal analgesia for thoracic surgeries. Numerous modalities have been studied: thoracic paravertebral nerve blocks, thoracic epidural analgesia, intercostal nerve blocks, patient controlled analgesia (PCA), cryo-analgesia, transcutaneous electrical nerve stimulation (TENS), inter-pleural blocks, stellate ganglion blocks, long thoracic nerve blocks, and infiltration under direct vision by the surgeon.

Serratus plane block is an emerging regional technique that has proven to be effective in comparison to paravertebral blocks in patients undergoing breast surgery and mastectomy with reduced perioperative opioid consumption and improved pain scores.

The lateral pectoral nerve, medial pectoral nerve, intercostal nerves and long thoracic nerve are all targets for the serratus plane block. It can be safely performed under ultrasound guidance.

The purpose of the study is to evaluate the difference in quality of analgesia between efficacy of serratus plane block and local surgical infiltration by surgeon as measured by patient opioid consumption and pain scores.

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Full Description

Participants will be assigned randomly using a computer-generated table of numbers to either serratus group or infiltration group. Block team will perform all blocks.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

ASA (American Society of Anesthesiology) class I-IV
age 81-75

Exclusion Criteria:

ASA class V
morbid obesity
patient refusal
patients with chronic pain or on pain medications
allergy to LA
patients receiving any additional regional techniques
coagulopathy
patients receiving systemic anticoagulation
local infection
procedures anticipated to last more than 5 hours.

Study is for people with:

Lung Cancer

Phase:

Phase 4

Estimated Enrollment:

65

Study ID:

NCT03642457

Recruitment Status:

Terminated

Sponsor:

Icahn School of Medicine at Mount Sinai

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There is 1 Location for this study

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Mount Sinai St. Luke's Hospital
New York New York, 10019, United States
Mount Sinai West Hospital
New York New York, 10019, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 4

Estimated Enrollment:

65

Study ID:

NCT03642457

Recruitment Status:

Terminated

Sponsor:


Icahn School of Medicine at Mount Sinai

How clear is this clinincal trial information?

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