Comparative Efficacy of Bifonazole Cream vs Placebo After Nail Ablation With Urea Paste
This study has been completed.
Sponsor:
Bayer
Information provided by:
Bayer
ClinicalTrials.gov Identifier:
NCT00781820
First received: October 28, 2008
Last updated: June 14, 2012
Last verified: June 2012
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
The study is focused to prove that the efficacy of a 1% Bifonazole cream is superior to a placebo cream after non-surgical nail ablation with a 40% urea paste.
| Condition | Intervention | Phase |
|---|---|---|
|
Onychomycosis |
Drug: Bifonazole cream 1% Drug: Placebo cream |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator) Primary Purpose: Treatment |
| Official Title: | A Double-blind, Randomized, Multicenter, Placebo- Controlled Phase 3 Trial to Prove the Superiority of Bifonazole vs. Placebo After 4 Weeks of Onychomycosis Treatment/ as a Follow-up of a 2 Weeks Treatment of Non-surgical Nail Ablation of Diseased Nail Matrix With 40% Urea Paste |
Resource links provided by NLM:
Further study details as provided by Bayer:
Primary Outcome Measures:
- Overall cure rate comprising clinical cure and mycological cure microscopy + culture negative [ Time Frame: 14 days after end of treatment (=visit 3) ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Clinical cure rate [ Time Frame: 14 days, 3 and 6 months after end of treatment (=visit 3, 4, and 5) ] [ Designated as safety issue: No ]
- Culture negative [ Time Frame: 14 days, 3 and 6 months after end of treatment (=visit 3, 4, and 5) ] [ Designated as safety issue: No ]
- Microscopy negative [ Time Frame: 14 days, 3 and 6 months after end of treatment (=visit 3, 4, and 5) ] [ Designated as safety issue: No ]
- Relapse rate (overall cure at visit 3 but positive clinical or mycological findings at visit 4 [ Time Frame: 3 and 6 months after end of treatment (=visit 4 and 5) ] [ Designated as safety issue: No ]
- Mycological cure rate (microscopy + culture negative) [ Time Frame: 3 and 6 months after end of treatment (=visit 4 and 5) ] [ Designated as safety issue: No ]
- Culture negative [ Time Frame: 6 months after end of treatment (=visit 5) ] [ Designated as safety issue: No ]
- Incidence of adverse events [ Time Frame: 2 weeks, 3 and 6 months after end of treatment (=visit 3, 4, and 5) ] [ Designated as safety issue: Yes ]
| Enrollment: | 693 |
| Study Start Date: | October 2008 |
| Study Completion Date: | January 2010 |
| Primary Completion Date: | January 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Placebo Comparator: Arm 2 |
Drug: Placebo cream
1 squeeze of Placebo cream sufficient to cover the infected nail bed(s) with a thin layer once daily for 28 days after nail ablation with urea paste
|
| Experimental: Arm 1 |
Drug: Bifonazole cream 1%
1 squeeze of Bifonazole cream sufficient to cover the infected nail bed(s) with a thin layer once daily for 28 days after nail ablation with urea paste
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Age of at least 18 years;
- Positive clinical findings of onychomycosis according to the judgement of the investigator (e.g. thickening, discoloration, structural changes, misshaped nails);
- Positive mycological findings (positive microscopy and positive culture with identification of pathogen) in material taken from affected nail sites before the start of treatment;
- Nail mycosis with an affected nail area between 20% and 50% in the target nail,
- Nail mycosis in not more than 3 nails (each nail not more than 50% infected area)
Exclusion Criteria:
- Doubtful or negative mycological findings;
- Proximal subungual onychomycosis (PSO);
- Topical antimycotic treatment of feet or hands within 4 weeks prior to screening, topical treatment of onychomycosis of feet or hands within 12 weeks prior to screening;
- Systemic antimycotic treatment within 12 weeks prior to screening;
- Failure to treat tinea pedis/manus (diagnosed at screening) successfully with topical treatment between screening visit and visit 1 (baseline);
- Tinea pedis/manus at visit 1 (baseline);
- Uncontrolled diabetes mellitus
- Psoriasis
- Peripheral arterial disease
- Chronic venous insufficiency;
- Diabetic neuropathy;
- History of hypersensitivity to bifonazole, or any other similar pharmacological agents or components of the products;
- Known sensitivity to plasters.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00781820
Hide Study Locations
Hide Study LocationsLocations
| Czech Republic | |
| Chomutov, Czech Republic, 43012 | |
| Hlinsko, Czech Republic, 539 01 | |
| Kutna Hora, Czech Republic, 28401 | |
| Louny, Czech Republic, 44001 | |
| Olomouc, Czech Republic, 77900 | |
| Praha, Czech Republic, 15500 | |
| Rychnov nad Kneznou, Czech Republic, 516 01 | |
| Slany, Czech Republic, 27401 | |
| Svitavy, Czech Republic, 56802 | |
| Usti nad Labem, Czech Republic, 40010 | |
| Germany | |
| Freiburg, Baden-Württemberg, Germany, 79104 | |
| Augsburg, Bayern, Germany, 86163 | |
| Augsburg, Bayern, Germany, 86179 | |
| Murnau, Bayern, Germany, 82418 | |
| Oberschleißheim, Bayern, Germany, 85764 | |
| Straubing, Bayern, Germany, 94315 | |
| Potsdam, Brandenburg, Germany, 14482 | |
| Frankenberg, Hessen, Germany, 35066 | |
| Marburg, Hessen, Germany, 35037 | |
| Hannover, Niedersachsen, Germany, 30159 | |
| Northeim, Niedersachsen, Germany, 37154 | |
| Aachen, Nordrhein-Westfalen, Germany, 52074 | |
| Dülmen, Nordrhein-Westfalen, Germany, 48249 | |
| Wuppertal, Nordrhein-Westfalen, Germany, 42275 | |
| Halle, Sachsen-Anhalt, Germany, 06108 | |
| Chemnitz, Sachsen, Germany, 09117 | |
| Dresden, Sachsen, Germany, 01277 | |
| Dresden, Sachsen, Germany, 01097 | |
| Leipzig, Sachsen, Germany, 04315 | |
| Löbau, Sachsen, Germany, 02708 | |
| Reichenbach, Sachsen, Germany, 08468 | |
| Lübeck, Schleswig-Holstein, Germany, 23558 | |
| Gera, Thüringen, Germany, 07551 | |
| Berlin, Germany, 13439 | |
| Berlin, Germany, 13597 | |
| Berlin, Germany, 13507 | |
| Berlin, Germany, 12157 | |
| Berlin, Germany, 10435 | |
| Berlin, Germany, 13055 | |
| Berlin, Germany, 10369 | |
| Berlin, Germany, 13437 | |
| Berlin, Germany, 10437 | |
| Berlin, Germany, 13187 | |
| Berlin, Germany, 10827 | |
| Hamburg, Germany, 20354 | |
| Poland | |
| Bialystok, Poland, 15-660 | |
| Gdansk, Poland, 80-177 | |
| Gdansk, Poland, 80-952 | |
| Olsztyn, Poland, 10-501 | |
| Pruszkow, Poland, 05-800 | |
| Wroclaw, Poland, 50-369 | |
Sponsors and Collaborators
Bayer
Investigators
| Study Director: | Bayer Study Director | Bayer |
More Information
Additional Information:
No publications provided
| Responsible Party: | Therapeutic Area Head, Bayer Consumer Care Inc. |
| ClinicalTrials.gov Identifier: | NCT00781820 History of Changes |
| Other Study ID Numbers: | 12999, 2008-003215-13 |
| Study First Received: | October 28, 2008 |
| Last Updated: | June 14, 2012 |
| Health Authority: | Germany: Federal Institute for Drugs and Medical Devices Czech Republic: State Institute for Drug Control Poland: Ministry of Health |
Keywords provided by Bayer:
|
Bifonazole Placebo Urea Nail fungus |
Additional relevant MeSH terms:
|
Onychomycosis Tinea Dermatomycoses Skin Diseases, Infectious Infection Mycoses Nail Diseases |
Skin Diseases Bifonazole Antifungal Agents Anti-Infective Agents Therapeutic Uses Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 22, 2013