Clinical Trials Directory

Trials / Completed

CompletedNCT05898607

Continuous Ultrasound Guided Erector Spinae Plane Block vs Thoracic Paravertebral Block

Continuous Ultrasound Guided Erector Spinae Plane Block vs Thoracic Paravertebral Block for Postoperative Analgesia in Patients Undergoing Thoractomy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Amal Gouda Elsayed Safan · Academic / Other
Sex
All
Age
21 Years
Healthy volunteers
Accepted

Summary

in this study the investigators will investigate and compare the analgesic efficacy of two techniques (continuous TPVB and continuous ESPB) in relieving thoracotomy pain

Detailed description

General Anesthesia will be induced with Fentanyl (1-2 μg/kg), Propofol (2-3 mg/kg), and Atracurium (0.5-0.8 mg/kg). Pressure controlled Volume guarantee Ventilation mode will be used to maintain O2 Saturation Above 98% and End tidal co2 Around 30-35 mmHg. Anesthesia will be maintained with Isoflurane 1.2 Minimum Alveolar Concentration inhalation after induction Group A: Patients will receive Loading dose of 20 ml 0.25% bupivacaine then continuous infusion U/S-Guided TPVB of 5 ml/h of 0.125% bupivacaine started through the catheter before the surgical procedure intraoperative and Group B: Patients will receive Loading dose of 20 ml 0.25% bupivacaine then continuous U/S-Guided ESPB of 5 ml/h of 0.125% bupivacaine started through the catheter before the surgical procedure intraoperative.

Conditions

Interventions

TypeNameDescription
OTHERcontinuous Thoracic paravertebral blockcontinuous infusion U/S-Guided TPVB of 5 ml/hr of 0.125% bupivacaine started through the catheter before the surgical procedure intraoperative.
OTHERcontinuous Erector spinae plane blockcontinuous U/S-Guided ESPB of 5 ml/hr of 0.125% bupivacaine started through the catheter before the surgical procedure

Timeline

Start date
2023-02-10
Primary completion
2023-10-10
Completion
2024-01-25
First posted
2023-06-12
Last updated
2024-01-26

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05898607. Inclusion in this directory is not an endorsement.