Overview
Perineural Dexmedetomidine for Ulnar Nerve Block.
Status:
Unknown status
Unknown status
Trial end date:
2018-04-01
2018-04-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The aim of this trial is to investigate if dexmedetomidine prolongs the duration of an ulnar nerve block. By using healthy volunteers the investigators can perform bilateral ulnar nerve blocks and thereby control for a systemic effect to clarify if the effect is actually peripheral or systemic. The investigators hypothesis is that dexmedetomidine as an adjunct to a local anaesthetic prolongs the duration of a peripheral nerve block by a peripheral mechanism.Phase:
Phase 2Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Zealand University HospitalTreatments:
Dexmedetomidine
Ropivacaine
Criteria
Inclusion Criteria:- Participants must understand the protocol fully and sign the written in-formed
consent.
- ASA 1-2
- BMI > 18 to < 30
- For fertile women: safe contraceptives for the last month and a nega-tive urin HCG.
Exclusion Criteria:
- Participants unable to cooperate in the trial.
- Participants unable to speak or read Danish
- Allergy to study medication.
- Alcohol consumption >21 units for men and >14 for women per week
- Daily intake of prescription painkillers within the last 4 weeks.
- Over the counter painkillers during the last 48 hours.
- Neuromuscular defects or wounds on the arms or hands preventing test performance.
- Diabetes Mellitus
- 2. degree heart block
- Sick sinus node.
- For fertile women a positive urine HCG