Pain treatment after planned hip surgery - effect of peripheral blockade of the obturator nerve

Phase 1

• Conditions: o specific medical condition is investigated. The objective of thetrial is to investigate a method for postoperative analgesia after elective hip surgery.; MedDRA version: 19.1Level: LLTClassification code 10068084Term: Anesthesia procedureSystem Organ Class: 100000004865; Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]

• Registration Number: EUCTR2017-000068-14-DK
• Lead Sponsor: Institut for Klinisk Medicin, Aarhus Universitet

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-04-18
• Last Update Posted: 23 July 2018

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

- Patients for primary hip replacement in spinal anesthesia
- Age >= 18 years
- American Society of Anesthesiologists physical status classification score I-III
- 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 30
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 30

Exclusion Criteria

- Lacking the ability to corporate
- Lacking the ability to speak danish
- Planned discharge on the same day of surgery
- Neuropathy of the lower extremities
- Contraindications for NonSteroidal Anti-Inflammatory Drugs (NSAID)
- Contraindications for dexamethasone
- Chronic opioid demanding pain
- Pregnancy
- Allergy towards the IMP
- Active treatment with amiodarone
- Active treatment with verapamil
- Active treatment with corticosteroids

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified