Trials / Unknown
UnknownNCT01113125
Scars After Central Venous Catheters
Topical Treatment With Glucocorticoids to Prevent Hypertrophic Scars and Keloid Due to Central Venous Access in Children
- Status
- Unknown
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Mette Møller Handrup · Academic / Other
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
Most children with cancer need a central venous catheter. These catheters are typically placed on the anterior thorax, where the risk of hypertrophic scarring and keloid development is greatly enhanced. A significant part of the children who have survived childhood cancer are troubled by their scars. Topical glucocorticoid treatment is known to induce a reduction of the collagen in the connective tissue. The investigators hypothesize that treatment with topical glucocorticoids for one week before and three weeks after removal of a central venous catheter, will reduce the formation of hypertrophic scarring and keloid development in children.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Betamethason-17-valerate and fusidic acid | 0.4 cm creme is applied and covered with a plaster (treatment under occlusion). Dosage every second or third day Treatment is started one week before removal of the central venous catheter and continued for four weeks |
| DRUG | Fusidic Acid | 0.4 cm creme is applied and covered with a plaster (treatment under occlusion). Dosage every second or third day Treatment is started one week before removal of the central venous catheter and continued for four weeks |
Timeline
- Start date
- 2010-03-01
- Primary completion
- 2014-08-01
- Completion
- 2016-07-01
- First posted
- 2010-04-29
- Last updated
- 2014-02-12
Locations
1 site across 1 country: Denmark
Source: ClinicalTrials.gov record NCT01113125. Inclusion in this directory is not an endorsement.