Analgesic Efficiency of Erector Spinae Plane Block Versus Thoracic Paravertebral Block in Patients Undergoing Lateral Thoracotomy Using Opoid Sparing Anesthesia
ESPvsTPVB
1 other identifier
interventional
86
1 country
1
Brief Summary
AimoftheWork To assess the efficiency of Opoid free anaesthesia with paravertebral block compared to opoid free anaesthesia with erector spinae plane block in patients undergoing Thoracotomy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 22, 2026
CompletedFirst Posted
Study publicly available on registry
February 27, 2026
CompletedStudy Start
First participant enrolled
March 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2026
ExpectedFebruary 27, 2026
February 1, 2026
3 months
February 22, 2026
February 22, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Total morphine consumption for the first 24 hours postoperative
Within the first 24 hours postoperative
Secondary Outcomes (1)
Postoperative pain
At 0,2,6,12,24 hours post operative
Study Arms (2)
Group A : thoracic para vertebral block
EXPERIMENTALPatients in this arm will receive ultrasound guided thoracic paravertebral block at the T5 level using 20 ml of 0.5% bupivacaine protocol for lateral thoracotomy
Group B : erector spinae plane block
EXPERIMENTALPatients in this arm will receive ultrasound guided erector spinae plane block at the T5 level using 20 ml of 0.5% bupivacaine as part of an opoid sparing anesthesia protocol for lateral thoracotomy
Interventions
Ultrasound guided thoracic paravertebral block performed at the T5 level using 20 ml of 0.5% bupivacaine for postoperative analgesia in patients undergoing lateral thoracotomy
ultrasound guided erector spinae plane block will be performed at the T5 level using 20 ml of 0.5% bupivacaine as part of an opoid sparing anesthesia protocol for lateral thoracotomy
Eligibility Criteria
You may qualify if:
- Patients age between 18 and 70 .
- Patients with ASAII and IIIstatus.
- Patients undergoing open surgical Thoracotomy as in lobectomy, pneumonectomy, segmentectomy and decortication.
- Gender both males and females.
- Refusal of the patient.
- Allergy to local anesthetic
- Infection of the skin at the site of local infiltration
- Cardiovascular problems (arrhythmia, heart block, SVT,AF, multiple extra systole).
- Any contraindication to regional anesthesia as coagulopathy
- Patients with chronic pain or on opoid medication preoperative
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Kasr al aini hospital
Cairo, Kasr Alaini, Egypt
Related Publications (4)
Doan LV, Augustus J, Androphy R, Schechter D, Gharibo C. Mitigating the impact of acute and chronic post-thoracotomy pain. J Cardiothorac Vasc Anesth. 2014 Aug;28(4):1048-56. doi: 10.1053/j.jvca.2014.02.021. No abstract available.
PMID: 25107721BACKGROUNDBenyamin R, Trescot AM, Datta S, Buenaventura R, Adlaka R, Sehgal N, Glaser SE, Vallejo R. Opioid complications and side effects. Pain Physician. 2008 Mar;11(2 Suppl):S105-20.
PMID: 18443635BACKGROUNDMarshall K, McLaughlin K. Pain Management in Thoracic Surgery. Thorac Surg Clin. 2020 Aug;30(3):339-346. doi: 10.1016/j.thorsurg.2020.03.001. Epub 2020 Apr 29.
PMID: 32593366BACKGROUNDMamoun N, Wright MC, Bottiger B, Plichta R, Klinger R, Manning M, Raghunathan K, Gulur P. Pain Trajectories After Valve Surgeries Performed via Midline Sternotomy Versus Mini-Thoracotomy. J Cardiothorac Vasc Anesth. 2022 Sep;36(9):3596-3602. doi: 10.1053/j.jvca.2022.05.007. Epub 2022 May 10.
PMID: 35641410RESULT
Central Study Contacts
Eman Mamdouh Mahmoud Hussien (emanmmh), Assistant lecturer
CONTACT
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer of anesthesia
Study Record Dates
First Submitted
February 22, 2026
First Posted
February 27, 2026
Study Start
March 1, 2026
Primary Completion
June 1, 2026
Study Completion (Estimated)
July 1, 2026
Last Updated
February 27, 2026
Record last verified: 2026-02