Local Anesthesia Clinical Trial
— REMIDOLCATHOfficial title:
REMIFENTANIL AND LOCAL ANESTHESIA COMPARED WITH LOCAL ANESTHESIA FOR THE INSERTION OF CENTRAL VENOUS CATHETERS IN AWAKE PATIENTS
Verified date | July 2020 |
Source | University Hospital, Toulouse |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
At present, there is no reference protocol for Central Venous Catheter (CVC) insertion assuring analgesia, anxiolysis and safety. Medical teams use various levels of analgesia and anesthesia to realize this gesture, from single local anesthesia to general anesthesia. Remifentanil has been shown to decrease pain scores for insertion and removal of long-term central venous access. Remifentanil is also often employed for pediatric or labor analgesia for short acts as procedural sedation.
Status | Completed |
Enrollment | 90 |
Est. completion date | December 2017 |
Est. primary completion date | December 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - more than 18 years old - eligible for CVC insertion Exclusion Criteria: - pregnancy - patients who can't give their consent - contra-indications to remifentanil infusion |
Country | Name | City | State |
---|---|---|---|
France | University Hospital of Toulouse | Toulouse |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Toulouse |
France,
Vardon Bounes F, Pichon X, Ducos G, Ruiz J, Samier C, Silva S, Sommet A, Fourcade O, Conil JM, Minville V. Remifentanil for Procedural Sedation and Analgesia in Central Venous Catheter Insertion: A Randomized, Controlled Trial. Clin J Pain. 2019 Aug;35(8) — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Maximal pain score on numeric rating scale (NRS) will be assessed after the insertion | up to 60 minutes | ||
Secondary | Evaluation of patient's anxiety by the Face Anxiety Scale | up to 60 minutes | ||
Secondary | Patient and physician's satisfaction by a 10-points numeric rating scale | up to 60 minutes | ||
Secondary | Number of adverse events | up to 60 minutes | ||
Secondary | Number of realized punctions | up to 60 minutes |
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