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NCT04855994 Clinical Trial

Comparison of Thoracic Paravertebral Block and Pectoral Nerve Block

Postoperative Analgesia Clinical Trial

Official title:
Comparison of the Results of Ultrasound-Guided Thoracic Paravertebral Block and Modified Pectoral Nerve Block for Postoperative Analgesia in Video-Assisted Thoracoscopic Surgery; A Prospective, Randomized Controlled Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04855994
Other study ID # 2017-140
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 28, 2017
Est. completion date August 28, 2018

Study information
Verified date July 2021
Source Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to compare the efficacy and safety of ultrasound-guidedPECS II block with TPVB for postoperative analgesia after VATS.

Description:

52 patients (ASA I-III) between 18 and 65 years of age, who were to undergo VATS, were randomized and divided into two groups. (26 patients in each of the PECS and TPVB groups) Thoracic paravertebral block was administered from two consecutive levels for TPVB group and a modified pectoral nerve block was performed in the PECS group. Postoperative analgesia was provided by intravenous morphine infusion using a patient-controlled analgesia device. Postoperative 24-hour total morphine consumption and duration of analgesia were the primary outcome measure. Perioperative remifentanil use, visual analog scale values during at rest and coughing, time of the first analgesic request, and additional analgesic consumption were recorded.

Recruitment information / eligibility
Status Completed
Enrollment 52
Est. completion date August 28, 2018
Est. primary completion date August 28, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Ages of 18-65 - Patients who will undergo VATS - ASA I-II-III patients Exclusion Criteria: - Patients with ASA IV - Clinically diagnosis of spinal or chest wall deformity or pathology - Clinically known local anesthetic allergy - Morbid obesity (body mass index>40 kg m2) - Clinically diagnosis of opioid, alcohol and substance dependence - Clinically diagnosis of psychiatric disease - Coagulopathy

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• paravertebral block
The investigators performed Paravertebral block to that patient group for postoperative analgesia
• pectoral block
The investigators performed pectoral block to that patient group for postoperative analgesia

Locations
Country Name City State
Turkey Bakirkoy Dr. Sadi Konuk Research and Training Hospital Istanbul Bakirkoy

Sponsors (1)
Lead Sponsor Collaborator
Bakirkoy Dr. Sadi Konuk Research and Training Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Postoperative 24-hours total morphine consumption of patients This will be measured only one time by pca device at the 24th hour after surgery. 24 hours postoperatively
Secondary Visual Analog Scale values of patients Visual Analog Scale (VAS, 0-10; 0= no pain and 10= very severe unbearable pain) at 0-1-2-4-8-12 and 24th hours 24 hours postoperatively
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