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Clinical Trials/NCT05852561
NCT05852561CompletedNot Applicable

Comparison of Combined Superficial and Deep Serratus Anterior Plan Block Versus Deep Serratus Anterior Plan Block for Postoperative Pain Control in Video-Assisted Thoracic Surgery

Ataturk University1 site in 1 country60 target enrollmentStarted: May 15, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
60
Locations
1
Primary Endpoint
Postoperative opioid consumption

Study Overview

Brief Summary

Thoracotomy is one of the most painful surgeries; Video-assisted thoracoscopic surgery (VATS) has been developed to reduce the surgical stress of thoracotomy. However, patients may experience moderate to severe pain within the first 24 hours after VATS. Intravenous opioids are frequently used to provide postoperative analgesia, and accordingly, side effects such as postoperative nausea/vomiting and respiratory depression can be seen.

The aim of this study is to compare Superficial+Deep Vs. Deep Serratus Anterior Plan Block for postoperative pain control in VATS cases.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •American Society of Anesthesiologist's physiologic state I-III patients
  • •To undergo Video Assisted Thoracic Surgery
  • •Being between the ages of 18-65 years

Exclusion Criteria

  • •having a known heart, kidney, liver or hematological disease
  • •having a history of peptic ulcer, gastrointestinal bleeding, allergy, chronic pain
  • •Routine analgesic use and history of analgesic use in the last 24 hours
  • •Not willingto participate in the study
  • •Uncooperative patients who have coagulopathy or use anticoagulant drugs
  • •To be allergic to one of the drugs to be used
  • •Contraindication for Video Assisted Thoracic Surgery

Arms & Interventions

Group Superficial+Deep Serratus Anterior Plan Block

Active Comparator

Superficial+Deep Serratus Anterior Plan Block after Video-Assisted Thoracic Surgery

Intervention: Group Superficial+Deep Serratus Anterior Plan Block (Other)

Group Deep Serratus Anterior Plan Block

Active Comparator

Deep Serratus Anterior Plan Block after Video-Assisted Thoracic Surgery

Intervention: Group Deep Serratus Anterior Plan Block (Other)

Outcomes

Primary Outcomes

Postoperative opioid consumption

Time Frame: first 24 hours

First 24 hours total fentanyl consumption with patient controlled analgesia

Secondary Outcomes

  • Visual analog pain score(first 48 hours)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Elif Oral Ahiskalioglu

Principal Investigator

Ataturk University

Study Sites (1)

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