Clinical Evaluation of DCB-WH1 in Healing of Chronic Diabetic Foot Ulcers
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|ClinicalTrials.gov Identifier: NCT00709514|
Recruitment Status : Completed
First Posted : July 3, 2008
Last Update Posted : July 9, 2013
The primary objective of this Phase 2 study is to evaluate the efficacy of DCB-WH1 ointment in wound closure as compared to vehicle control when applied topically to chronic diabetic foot ulcers for 12 weeks. The secondary objective of this study is to collect safety information of DCB-WH1 ointment.
This is a randomized, double-blind, parallel group, vehicle-controlled, multi-center study of DCB-WH1 ointment applied topically to grade 1 foot ulcers (according to Wagner grading system) in 50 subjects with diabetes mellitus.
|Condition or disease||Intervention/treatment||Phase|
|Chronic Diabetic Foot Ulcer||Drug: DCB-WH1 ointment Drug: Placebo||Phase 2|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||41 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||A Phase II, Double-blind, Placebo-controlled Clinical Evaluation of DCB-WH1 in Healing of Chronic Diabetic Foot Ulcers|
|Study Start Date :||December 2008|
|Actual Primary Completion Date :||April 2011|
|Actual Study Completion Date :||March 2012|
Experimental: DCB-WH1 ointment
DCB-WH1 ointment 1.25%, topical use, two times daily for 12 weeks or until ulcer closes completely or discontinuation due to treatment failure, whichever comes first.
Drug: DCB-WH1 ointment
DCB-WH1 ointment (1.25%), topically applied twice daily
Placebo Comparator: Placebo
Placebo, topical use, two times daily for 12 weeks or until ulcer closes completely or discontinuation due to treatment failure, whichever comes first.
- The incidence of complete ulcer closure [ Time Frame: 12 weeks ]
- The time of healing rate and change in ulcer area [ Time Frame: 12 weeks ]time to ulcer closure, time to half ulcer closure, ulcer closure rate at endpoint, change and percentage change from baseline in ulcer size
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00709514
|Clinical Research Division|
|Taipei, Taiwan, 115|
|Principal Investigator:||Low-Tong Ho, MD||Taipei Veterans General Hospital Taipei|