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Clinical Trials/EUCTR2020-005443-23-ES
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.

Registry
who.int
Start Date
July 5, 2021
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Hospital Sant Joan de Reus

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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