Evaluation of the Effect of Vivostat Platelet Rich Fibrin(PRF) in the Treatment of Diabetic Foot Ulcers

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00770939
Recruitment Status : Completed
First Posted : October 10, 2008
Last Update Posted : October 12, 2011
Information provided by (Responsible Party):

October 9, 2008
October 10, 2008
October 12, 2011
July 2008
May 2010   (Final data collection date for primary outcome measure)
  • Proportion of completely healed ulcers after 12 weeks [ Time Frame: 12 weeks ]
  • Percentage of patients with a 50% reduction of wound area after 4 and 8 weeks [ Time Frame: 8 weeks ]
Same as current
Complete list of historical versions of study NCT00770939 on Archive Site
Granulation rate [ Time Frame: 12 weeks ]
Same as current
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Evaluation of the Effect of Vivostat Platelet Rich Fibrin(PRF) in the Treatment of Diabetic Foot Ulcers
A Cohort Study to Evaluate the Effect of Vivostat Platelet Rich Fibrin on Diabetic Foot Ulcers.

Diabetic foot ulcers are a challenge to health care professionals because there are only few effective topical therapeutic interventions.

Growth factor treatment has shown to be beneficial for healing of diabetic foot ulcers in conjunction with extensive surgical debridement. Autologues platelet releasate which contains platelet derived growth factor appears to be more effective than standard therapy in case studies.

This protocol will evaluate the healing effect of Vivostat PRF treatment of non-eschemic foot ulcers to identify responders and to enable sample size calculation for a subsequent pivotal trial.

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Phase 4
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Diabetic Foot Ulcers
Device: Vivostat PRF
Ulcer will be treated week 1,2,3,4,5 and 6 with Vivostat PRF
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*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
Same as current
August 2010
May 2010   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • At least 4 weeks history (with wound area measurements) within a wound care institution before the first visit (week -3). In case of referral the patient history must be documented
  • All patients must complete a 3 week screening period i.e. they will be interviewed and accessed at the first meeting. During the 3 week period patient compliance will be monitored.
  • Age >18 years
  • Type I or Type II Diabetes Mellitus
  • Ulcer at or below the ankle which has been present for at least 4 weeks, and has received best practice care
  • Ulcer area between 0,5 and 16 cm2
  • If there is more than one ulcer or bilateral ulcers, the investigator shall choose the one index ulcer to be treated (typically the largest one). The other ulcers will receive standard care and is not included in the study
  • Ulcer type: University of Texas grade IA.
  • Evidence of adequate arterial perfusion: Toe pressure reading of ≥ 30 mmHg or if toe is missing, transcutaneous oxygen (TcPO2) of ≥ 30mmHg on the foot.
  • Patient foot is appropriately off loaded (contact cast, pneumatic walking cast)
  • Orthopaedic assessment has been completed to rule out a mechanical source of ulceration
  • Relative wound area reduction less than 50% from week -3 to week 0 (pre-screening period)
  • Signed informed consent

Exclusion Criteria:

  • Clear indication for surgery (vascular reconstruction or skin transplant)
  • Ulcer with exposed bone or tendon
  • Bone involvement (probe to bone or x-ray)
  • Patients with 3 ulcers or more at the foot investigated
  • Osteomyelitis
  • Clinical signs of infections
  • Necrosis in the wound (one week into the screening period).
  • Patients with known MRSA
  • Malnutrition. Albumin < 2,5g/dl
  • Ulcers resulting from electrical, chemical, radiation burns
  • HbA1c > 12%
  • Male: Hb < 8 mmol/l (12,9 g/dlFemale: Hb < 7 mmol/l (11,3 g/dl)
  • Platelet count <140 *109/l
  • Pregnancy and fertile women not practicing sufficient birth control
  • Fertile women having a positive pregnancy test week 0 Lactating women
  • Patients on haemodialysis
  • History of peripheral vascular repair within 4 weeks prior to study enrollment
  • Bleeding disorders, haemophilia, sickle cell disease, thrombocytopenia, and leukaemia or blood dyscrasias
  • Current treatment for malignancy or neoplastic disease or collagen vascular disease
  • Highly communicable disease or diseases that may limit follow - up (e.g. immunocompromised conditions, hepatitis, active tuberculosis)
  • Patient has inadequate venous access to draw blood
  • History of alcohol or drug abuse within the last year prior to randomization
  • Patient known to have psychological, developmental, physical, emotional or social dis-order or other ailments that may interfere with the study requirements
  • Patients enrolled in an other clinical trial for wound treatment within 30 days prior to enrollment
  • Non-compliance in the screening period
  • Patients who have received growth factor therapy e.g. becaplermin within 7 days prior to enrollment
Sexes Eligible for Study: All
18 Years and older   (Adult, Older Adult)
Contact information is only displayed when the study is recruiting subjects
Denmark,   Germany,   Sweden
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Study Director: Michael Ruge Vivostat
October 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP