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Sensory distribution of lateral femoral cutaneous nerve block - a randomised, blinded, paired trial in heathy volunteers

Phase 1
Conditions
Healthy volunteers (treatment intended for pain treatment in patientsafter hip surgery)
MedDRA version: 19.0Level: LLTClassification code 10054711Term: Postoperative painSystem Organ Class: 100000004863
Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
Registration Number
EUCTR2016-002643-41-DK
Lead Sponsor
Department of Anesthesiology, Næstved Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Age >18
ASA 1-2
BMI >18 and < 30
Written informed consent
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 20
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Allergy to study medication
Alcohol consumption >21 units of alcohol per week
Medical abuse (as judged by investigator)
Daily intake of perscription painkillers within the last 4 weeks
Intake of over the counter medication within 48 hours
Earlier trauma, neuromusclare diseases, or surgery to lower limb
Diabetes mellitus
Cant cooperate
Cant speak or understand danish
Pregnant women

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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