The Ehlers-Danlos syndrome and regional anesthesia.
Recruiting
- Conditions
- The Ehlers-Danlos syndrome, locoregional anesthesia. <br />Het Ehlers-Danlos syndroom, cutis hyperelastica, locoregionale anesthesie
- Registration Number
- NL-OMON22447
- Lead Sponsor
- sponsor: A.J.M. van Wijck, MD PhD, department of anesthesiology, UMC Utrecht<br><br>principal investigator: J.C. Mier, MD, department of anesthesiology, UMC Utrecht
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
For the Ehlers-Danlos group:
1. people with all types of Ehlers-Danlos except type IV, proven by a geneticist or a comparably qualified person;
Exclusion Criteria
For Ehlers-Danlos patients:
1. Type IV Ehlers-Danlos;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Analgesia in the region of the ulnar nerve within 60 minutes after application of an ulnar nerve block.This will be demonstrated by increasing stimuli from a neurostimulator. If the subject does not regard 20 mA as painful there is of an adequate block.
- Secondary Outcome Measures
Name Time Method Analgesia from the subcutanous injections and the topical application of EMLA cream. Time of onset of analgesia. Time of end of analgesia. Duration of analgesia.