Clinical Trials Directory

Trials / Unknown

UnknownNCT00446472

Evaluation of Windowed Casts With and Without Regranex® Gel for Healing Diabetic Neuropathic Ulcers

Evaluation of Windowed Casts With and Without Regranex® Gel for Healing

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Southern California Institute for Research and Education · Academic / Other
Sex
All
Age
21 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to compare the effectiveness and safety of windowed casts with Regranex® (topical becaplermin gel) versus placebo (inactive medication) for treatment of diabetic ulcers on the legs and feet.

Detailed description

Management of diabetic leg or foot ulcers is based on certain principals: 1) effective off-loading of pressure on the wound via specialized shoes, cast braces, or casts, 2) removal of infected or necrotic tissue vial surgery or non-surgical methods, and 3) optimization of wound healing by interventions that promote wound repair such as nutritional support, provision of optimal moisture balance and growth factor therapy. Application of casts or cast braces \[below knee, removable boots with protective padding\] to protect and immobilize the ankle and foot have been demonstrated to provide superior wound healing than less cumbersome types of shoe gear (1-3). The benefit of casting may be the result of more effective off-loading of pressure than can be achieved with other devices, but the inability of patients to remove their casts also appears to an important factor, as non-compliance with removable cast-braces has been shown to be a pervasive and significant issue (4,5). One critical concept in diabetic foot ulcer management is the relation between chronically and limb loss - for each year a wound persists, a patient has a 25% risk for major amputation due to complications from infection (6-8). Limb loss has a profound effect on Diabetics' quality of life and rate of lower limb loss among diabetics is four per 1,000 person years in comparison with three per 10,000 person years (9-10).

Conditions

Interventions

TypeNameDescription
DRUGRegranex®Regranex gel will be used for a total of 16 weeks
DRUGHydrogelPlacebo hydrogel will be applied for 16 weeks

Timeline

Start date
2007-04-01
Primary completion
2010-09-01
Completion
2010-09-01
First posted
2007-03-12
Last updated
2010-06-04

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00446472. Inclusion in this directory is not an endorsement.