Status:
COMPLETED
PECS II Block in Thoracic Outlet Decompression
Lead Sponsor:
Catharina Ziekenhuis Eindhoven
Conditions:
Thoracic Outlet Syndrome
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Rationale: Postoperative pain management after transaxillary thoracic outlet decompression surgery (TATOD) is difficult. In a retrospective case-control trial, we found evidence that a PECS II block i...
Eligibility Criteria
Inclusion
- Patients with NTOS
- Selected for a trans-axillary thoracic outlet decompression (TATOD) by the TOS multidisciplinary workgroup.
- Fit for surgery, defined as ASA (American Society of Anesthesiologists) Classification of I, II or III.
- 18 years of age or older
- Sufficient in speaking and writing the Dutch language
- Normal liver and renal function
- Informed consent
Exclusion
- Patients with a history of TOD (Redo-surgery)
- Patients with ATOS or VTOS
- ASA ≥ 4
- Kidney or liver failure with contra-indication for NSAID or paracetamol
- Mental retardation
- Pregnancy
- Patients with chronic strong opioid use (\>3 administrations per week or continuous transdermal therapy, longer than the last 3 months)
- Allergy to one or more medications used in the study including, ropivacaine, dexamethasone, propofol, sufentanil, succinylcholine, paracetamol, NSAID, morphine, granisetron
- Patients that have trouble expressing themselves in Dutch. Questionnaires are completed by the patients and checked by the nurses. The questionnaire is in Dutch. If there is a language barrier between the questionnaire, the patient or the health care worker, we believe the validity of the answers is questionable.
Key Trial Info
Start Date :
August 27 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 3 2021
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT04471545
Start Date
August 27 2020
End Date
October 3 2021
Last Update
March 10 2022
Active Locations (1)
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1
Catharina Ziekenhuis
Eindhoven, North Brabant, Netherlands, 5623 EJ