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
| Type | Name | Description |
|---|---|---|
| DRUG | Hirudoid cream 0.3 % Mucopolysaccharide polysulfate | Hirudoid cream |
| DRUG | Placebo 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.