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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
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05898607
Enrollment
40
Registered
2023-06-12
Start date
2023-02-10
Completion date
2024-01-25
Last updated
2024-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Brief 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.

Interventions

continuous infusion U/S-Guided TPVB of 5 ml/hr of 0.125% bupivacaine started through the catheter before the surgical procedure intraoperative.

continuous U/S-Guided ESPB of 5 ml/hr of 0.125% bupivacaine started through the catheter before the surgical procedure

Sponsors

Mohamed Emad Basune
CollaboratorUNKNOWN
Wesam Eldin Sultan
CollaboratorUNKNOWN
Rabab Mohammed Habeeb
CollaboratorUNKNOWN
Amal Gouda Elsayed Safan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

\- Eligible 40 patients will be older than 21 years old with American society of anesthesia physical status I& II scheduled for elective thoracotomy

Exclusion criteria

* Patients who are: * Uncooperative. * Having allergy to any of the study drugs. * Known abuse of alcohol or medication. * Having Local infection at the site of injection or systemic infection. * Pregnancy. * With coagulation disorders or on anticoagulation therapy

Design outcomes

Primary

MeasureTime frameDescription
Compare the VAS score postoperative of (U/S)-guided continuous (ESPB) to continuous (TPVB) following thoracotomy48 hoursvisual analogue scale (VAS) Score

Secondary

MeasureTime frameDescription
1 st call analgesia1 hourmg
Total rescue opioid dose used48 hourmg
patient satisfaction at 24 hours24 hours
occurrence of adverse events24hours
hospital stay1 weekdays

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026