The Impact of Video-assisted Thoracic Surgery and Regional Anaesthesia on Postoperative Opioid Consumption and Pain Scores

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorAntalya Training and Research Hospital

About this trial

This present study aims is to compare the effects of ultrasound-guided paravertebral block, intertransverse process block, and erector spinae plane block on postoperative opioid consumption, and pain scores in patients undergoing VATS.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

aged 18-75 years

American Society of Anaesthesiology (ASA) score I-III

body mass index (BMI) <35kg/m2

scheduled for elective VATS

Disqualifiers

ASA score ≥4

BMI ≥35 kg/m2

declining to give written informed consent

controendications for block application

Trial population

It is planned to include ASA score I-III adult patients who are planned to undergo elective VATS

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • Paravertebral block group

    Other intervention

    Before the surgery, ultrasoud-guided paravertebral block will be performed before the surgery under standart anaesthesia monitoring

  • İntertransverse process block group

    Other intervention

    Before the surgery, ultrasoud-guided intertransverse process block will be performed before the surgery under standart anaesthesia monitoring

  • Erector spinae plane block group

    Other intervention

    Before the surgery, ultrasoud-guided erector spinae plane block will be performed before the surgery under standart anaesthesia monitoring

Treatment groups

96 Participants
are divided into 3 treatment groups
Group A: Paravertebral block group1 intervention
Group B: İntertransverse process block group1 intervention
Group C: Erector spinae plane block group1 intervention

Trial outcomes

Primary outcomes

1

Postoperative opioid consumption

All patients will receive a standard patient analgesia (PCA) protocol after operation. The postoperative opioid consumption will only be recorded.

Time frame
24 hours

Secondary outcomes

1

Postoperative Numerical Rating Scale (NRS) pain scores

The postoperative pain intensity will be assessed with the Numerical Rating Scale (NRS) score (0=no pain; 10=most severe pain).

Time frame
postoperative 24 hours
2

Chronic pain

Patients will be telephoned 3 months after the surgery and the presence, localization, intensity of the pain , its character, and its relation with rest and/or activity will be recorded by asking only verbally.

Time frame
3 months

Other outcomes

Sponsors and contacts

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