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OpenTrials
Completed

NCT Number: NCT04999319

Morphine Consumption in Thoracotomy

Importance of effective postoperative pain management is well known. The undesired effects of pain can be prevented with multimodal analgesia for the patient. Thoracotomy operations are associated with high levels of pain. With the use of ultrasound, many regional anesthesia techniques were described to provide effective postoperative analgesia. The aim of this study was to compare the postoperative effect of paravertebral block (PVB) and erector spinal plane block (ESPB) in thoracotomies.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kocaeli Unversity

Kocaeli, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ASA I-III patients undergo elective thoracotomy surgeries.

Exclusion criteria

  • Obesity (BMI > 35 kg/m2)
  • Infection of the skin at the site of the needle puncture area
  • Patients with known allergies to any of the study drugs
  • Coagulopathy

Treatment and study plan

PVB

Procedure

Paravertebral block will be performed before the surgery with 20 mL of %0.5 bupivacaine at T4 level.

ESPB

Procedure

Erector spinae plane block will be performed before the surgery with 20 mL of %0.5 bupivacaine at T4 level.

Primary outcomes

  1. Morphine consumption

    Time frame: Postoperative 24th hour

    Morphine consumption (mg) of patients with patient controlled analgesia device

  2. NRS score

    Time frame: Postoperative 24th hour

    Numerating rating scale of the patients (between 0 and 10, 0 represents no pain and 10 represents the worst pain ever possible.

Sponsors and collaborators

Lead sponsor

Kocaeli University

Other

Registry information

Official study title

Comparison of Morphine Consumption at Postoperative 24th Hour in Thoracotomy: A Randomized Controlled Trial

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Aug 10, 2021
Registry last updated
Jan 26, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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