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Tissue Adhaesive in Wound Closure Following Primary Total Knee Arthroplasty

NCT03289247 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2019-01-25

No results posted yet for this study

Summary

The study's primary objective is to compare the following parameters between wound closure following primary TKA with and without supplement tissue adhesive (Leukosan®):

Conditions

  • Total Knee Arthroplasty
  • Infection
  • Arthroplasty Complications

Interventions

DEVICE

tissue adhesive (Leukosan®)

Tissue ahaesive

Sponsors & Collaborators

  • Hvidovre University Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-09-01
Primary Completion
2017-12-21
Completion
2018-12-31

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03289247 on ClinicalTrials.gov