- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06563557
Erasme Randomized Controlled Trial Surveys Hemodynamic Excursions During Esophagectomy (ERASME ULB)
August 19, 2024 updated by: Erasme University Hospital
ERASME ULB: Erasme Randomized Controlled Trial Surveys Hemodynamic Excursions During Esophagectomy - a Double Blind Study
In our high volume center, the majority of esophagectomy procedures are performed with minimally invasive techniques.
The thoracic epidural technique remains the gold standard and homolateral paravertebral catheter is strongly recommended.
The vasoplegia and sympathetic blockade due to the epidural can cause significant hypotension especially as reverse Trendelenburg position is required during surgery.
The aim is to study hemodynamic changes caused by two different techniques.
Previous studies found a similar pain management between both locoregional techniques, however few studies suggested less side effects in the paravertebral group during major abdominal surgeries.
Study Overview
Status
Not yet recruiting
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
75
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Annalinda CIORRA, MD
- Phone Number: +32(0)25553324
- Email: annalinda.ciorra@hubruxelles.be
Study Contact Backup
- Name: Fanny BERNARD, MD
- Phone Number: +32(0)25553324
- Email: fanny.bernard@hubruxelles.be
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Adult, Capable of giving consent, two or three incisions esophagectomy (thoracoscopic/ thoracotomy) no laparotomy
Exclusion Criteria:
- patient refusal, total language barrier, coagulation disorders, thrombocytopenia <75 000, contraindications to locoregional anesthesia (infection local site, allergy to local anesthesic), scoliosis Cobb > 45%, atrial fibrillation, end stage renal disease),
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Epidural group
|
The thoracic epidural technique remains the gold standard for perioperative pain management for this procedure.
The placement of a paravertebral catheter homolateral with the thoracic incisions is strongly recommended.
A goal directed fluid therapy is proposed to guide fluid management and limit postoperative complications.
Few studies suggested less side effects in the paravertebral group.
The vasoplegia due to the epidural can cause significant hypotension especially as reverse Trendelenburg position is required during surgery.
The aim is to bring more light to the hemodynamic changes caused by two different locoregional techniques.
An algorithm for fluid and vasopressor management has been proposed.
We defined hypotension as 20% of decrement of the median arterial pressure during anesthesia.
To reduce bias, the locoregional techniques is performed by an experienced anesthesiologists and the rest of the perioperative management is conducted by another blinded anesthesiologist.
|
|
Experimental: Paravertebral group
|
The thoracic epidural technique remains the gold standard for perioperative pain management for this procedure.
The placement of a paravertebral catheter homolateral with the thoracic incisions is strongly recommended.
A goal directed fluid therapy is proposed to guide fluid management and limit postoperative complications.
Few studies suggested less side effects in the paravertebral group.
The vasoplegia due to the epidural can cause significant hypotension especially as reverse Trendelenburg position is required during surgery.
The aim is to bring more light to the hemodynamic changes caused by two different locoregional techniques.
An algorithm for fluid and vasopressor management has been proposed.
We defined hypotension as 20% of decrement of the median arterial pressure during anesthesia.
To reduce bias, the locoregional techniques is performed by an experienced anesthesiologists and the rest of the perioperative management is conducted by another blinded anesthesiologist.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Consumption of norepinephrine and fluids during procedure
Time Frame: 6 hours
|
norepinephrine mcg/kg/hr
|
6 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postoperative complications
Time Frame: 6 months
|
Medical complications: Pneumonia, atrial fibrillation, thromboembolic event Surgical complications : Wound dehiscence, anastomotic leakage, chylothorax, recurrent laryngeal nerve injury
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Laszlo SZEGEDI, PHD, Laszlo.szegedi@hubruxelles.be
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Low DE, Allum W, De Manzoni G, Ferri L, Immanuel A, Kuppusamy M, Law S, Lindblad M, Maynard N, Neal J, Pramesh CS, Scott M, Mark Smithers B, Addor V, Ljungqvist O. Guidelines for Perioperative Care in Esophagectomy: Enhanced Recovery After Surgery (ERAS(R)) Society Recommendations. World J Surg. 2019 Feb;43(2):299-330. doi: 10.1007/s00268-018-4786-4.
- Yeung JH, Gates S, Naidu BV, Wilson MJ, Gao Smith F. Paravertebral block versus thoracic epidural for patients undergoing thoracotomy. Cochrane Database Syst Rev. 2016 Feb 21;2(2):CD009121. doi: 10.1002/14651858.CD009121.pub2.
- Deana C, Vetrugno L, Bignami E, Bassi F. Peri-operative approach to esophagectomy: a narrative review from the anesthesiological standpoint. J Thorac Dis. 2021 Oct;13(10):6037-6051. doi: 10.21037/jtd-21-940.
- Kingma BF, Eshuis WJ, de Groot EM, Feenstra ML, Ruurda JP, Gisbertz SS, Ten Hoope W, Marsman M, Hermanides J, Hollmann MW, Kalkman CJ, Luyer MDP, Nieuwenhuijzen GAP, Scholten HJ, Buise M, van Det MJ, Kouwenhoven EA, van der Meer F, Frederix GWJ, Cheong E, Al Naimi K, van Berge Henegouwen MI, van Hillegersberg R. Paravertebral catheter versus EPidural analgesia in Minimally invasive Esophageal resectioN: a randomized controlled multicenter trial (PEPMEN trial). BMC Cancer. 2020 Feb 22;20(1):142. doi: 10.1186/s12885-020-6585-1.
- van den Berg JW, Tabrett K, Cheong E. Paravertebral catheter analgesia for minimally invasive Ivor Lewis oesophagectomy. J Thorac Dis. 2019 Apr;11(Suppl 5):S786-S793. doi: 10.21037/jtd.2019.03.47.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
August 1, 2024
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
December 12, 2026
Study Registration Dates
First Submitted
August 19, 2024
First Submitted That Met QC Criteria
August 19, 2024
First Posted (Actual)
August 21, 2024
Study Record Updates
Last Update Posted (Actual)
August 21, 2024
Last Update Submitted That Met QC Criteria
August 19, 2024
Last Verified
June 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- P2023/514 /B4062024000032
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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