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Trials / Completed

CompletedNCT01943006

Efficacy and Tolerability of Hirudoid Cream in Prophylaxis and Treatment Infusion Phlebitis

Efficacy and Tolerability of Hirudoid Cream in Prophylaxis and Treatment of Superficial Infusion Thrombophlebitis

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
144 (actual)
Sponsor
Medinova AG · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Patients receiving nutritional emulsion for at least 3 days will be treated with Hirudoid cream or placebo cream to prevent and treat phlebitis caused by the infusion. The treatment is continued after the end of infusion for at least 7 days. Number of patients developing superficial phlebitis and duration of phlebitis will be recorded.

Conditions

Interventions

TypeNameDescription
DRUGHirudoid cream 0.3 % Mucopolysaccharide polysulfateHirudoid cream
DRUGPlacebo cream without active substance

Timeline

Start date
2015-05-01
Primary completion
2017-02-01
Completion
2017-03-01
First posted
2013-09-16
Last updated
2017-12-14

Locations

4 sites across 1 country: Thailand

Source: ClinicalTrials.gov record NCT01943006. Inclusion in this directory is not an endorsement.

Efficacy and Tolerability of Hirudoid Cream in Prophylaxis and Treatment Infusion Phlebitis (NCT01943006) · Clinical Trials Directory