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RECRUITING
NCT02652169
NA

PRF With Topical Antibiotics or Antiseptics in Chronical Wounds Version 1.4

Sponsor: Medical University of Vienna

View on ClinicalTrials.gov

Summary

Platelet rich fibrin (PRF) is a new therapy option for chronic wounds with yet unproven therapeutic efficacy. This randomised controlled trial aims to provide evidence of the efficacy of PRF as monotherapy as well as a growth promoting carrier matrix for antimicrobial compounds. The investigators therefore designed a four armed trial with three PRF arms which are compared to each other as well as to an active comparator. The treatment arms are as follows: Study arm 1: PRF with amikacin and teicoplanin Study arm 2: PRF with placebo (0.9% sodium chloride) Study arm 3: PRF with PHMB (polyhexanid) plus Macrogolol (Lavasorb®) Study arm 4: Acticoat 7® wound dressing as active control Patients with infected chronic wounds may be included in this trial. Infection shall be diagnosed by an experienced senior infectious diseases specialist. Patients with untreated peripheral vascular occlusive disease as defined by an ABI (ancle brachial index) of \< 0,7 are excluded from the trial as are patients with an uncontrolled diabetes mellitus or patients who have not received sufficient treatment for a diabetic foot syndrome. Any underlying illness will be treated following standard of care. In case of chronic venous insufficiency four-layered compression bandages will be applied each visit if tolerated by the patient. Alternatively compression stockings (Class III) are permitted. This is mentioned as "Disease specific treatment" in the protocol. Patients will receive treatment for 56 days. After 28 and 56 days the wound surface will be compared to the baseline. Infection parameters (c-reactive protein and leucocyte count) will be measured weekly. Evaluation of systemic antimicrobial therapy will be performed at each visit. Systemic antimicrobial therapy is started at the discretion of a senior infectious diseases specialist.

Official title: Platelet Rich Fibrin in Combination With Topical Antibiotics or Antiseptics in the Treatment of Chronic Wounds - a Prospective, Randomized, Active Controlled, Double Blind Pilot Trial With an Observer-blinded Control Group

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

120

Start Date

2014-06

Completion Date

2027-04

Last Updated

2022-04-07

Healthy Volunteers

No

Interventions

DRUG

PRF mixed with amikacin and teicoplanin

PRF, mixed with amikacin and teicoplanin is applied to the chronic ulcer

DRUG

PRF mixed with PHMB plus Macrogolol

PRF, mixed with Lavasorb is applied to the chronic ulcer

DRUG

PRF plus normal saline

PRF as a monosubstance plus sodium chloride 0.9% is applied to the chronic ulcer

OTHER

Silver gauze

Acticoat 7 silver wound dressing is applied to the chronic ulcer

Locations (1)

Medical University of Vienna

Vienna, Austria