Shamrock versus Lumbar Ultrasound Trident – Ultrasound guided block of the lumbar nervous plexus
- Conditions
- MedDRA version: 17.1Level: LLTClassification code 10054710Term: Postoperative hip painSystem Organ Class: 100000004863MedDRA version: 17.1Level: PTClassification code 10051060Term: Hip surgerySystem Organ Class: 10042613 - Surgical and medical proceduresTherapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
- Registration Number
- EUCTR2013-005346-10-DK
- Lead Sponsor
- Thomas Fichtner Bendtsen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- Male
- Target Recruitment
- Not specified
• Male.
• Age = 18 years.
• Volunteers who have given their written and oral informed consent to participate in the study after fully understanding the content and the limitations of the protocol.
• Normal healthy person (American Society of Anesthesiology Classification, ASA I).
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
• Volunteers not able to cooperate for the study.
• Volunteers not able to understand Danish.
• Daily use of analgesics.
• Allergy against the medicines used in the study.
• Drug abuse – according to the investigator's judgement
• Alcohol consumption larger than the recommendations of the Danish National Board of Health
• Volunteers in who nerve blocks are not possible due to technical reasons
• Volunteers who fulfil any contraindiation for MRI including claustrophobia.
• Volunteers who are incompetents, eg. surrogate consent is not accepted.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method