Morphine Consumption in Thoracotomy

Postoperative Pain Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04999319
• Other study ID #: GOKAEK-2020/18.09
• Status: Completed
• Phase: N/A
• Start date: October 15, 2020
• Est. completion date: January 25, 2022

Study information

• Verified date: January 2022
• Source: Kocaeli University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44
• Est. completion date: January 25, 2022
• Est. primary completion date: January 5, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

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

Related Conditions & MeSH terms

• Pain, Postoperative
• Postoperative Pain

Intervention

Procedure:
• PVB
Paravertebral block will be performed before the surgery with 20 mL of %0.5 bupivacaine at T4 level.
• ESPB
Erector spinae plane block will be performed before the surgery with 20 mL of %0.5 bupivacaine at T4 level.

Locations

Country	Name	City	State
Turkey	Kocaeli Unversity	Kocaeli

Sponsors (1)

Lead Sponsor	Collaborator
Kocaeli University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Morphine consumption	Morphine consumption (mg) of patients with patient controlled analgesia device	Postoperative 24th hour
Primary	NRS score	Numerating rating scale of the patients (between 0 and 10, 0 represents no pain and 10 represents the worst pain ever possible.	Postoperative 24th hour