EUCTR2020-005443-23-ES
Active, not recruiting
Phase 1
Comparative study between two ultrasound-guided peripheral blocks for postoperative analgesia of primary total knee arthroplasty
Hospital Sant Joan de Reus0 sites60 target enrollmentJuly 5, 2021
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Hospital Sant Joan de Reus
- Enrollment
- 60
- Status
- Active, not recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •The included patients will undergo unilateral primary total knee arthroplasty, aged between 50 and 80 years, ASA I\-III, BMI \<35 kg / m2, with no previous history of adverse effects and / or allergy to local anesthetics, NSAIDs , metamizole or tramadol, without psychiatric pathology, with correct cognitive capacity, as well as the understanding and written consent of their participation in this study.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) no
- •F.1\.2\.1 Number of subjects for this age range
- •F.1\.3 Elderly (\>\=65 years) yes
- •F.1\.3\.1 Number of subjects for this age range 60
Exclusion Criteria
- •Those patients with indication for primary total knee arthrosplasty with decompensated systemic diseases (hyperthyroidism, severe peripheral vascular disease, diabetics ...), prosthetic replacement surgeries, uncontrolled psychiatric disorders, denial or contraindication to intradural regional anesthesia and peripheral, with a previous history of adverse effects and / or allergy to local anesthetics, NSAIDs, metamizole or tramadol.
Outcomes
Primary Outcomes
Not specified
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