Controlled Nitric Oxide Releasing Patch Versus Meglumine Antimoniate in the Treatment of Cutaneous Leishmaniasis
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Purpose
Cutaneous leishmaniasis is a worldwide disease, endemic in 88 countries, that has shown an increasing incidence over the last two decades. So far, pentavalent antimony compounds have been considered the treatment of choice, with a percentage of cure of about 85%. However, the high efficacy of these drugs is counteracted by their many disadvantages and adverse events. Previous studies have shown nitric oxide to be a potential alternative treatment when administered topically with no serious adverse events. However, due to the unstable nitric oxide release, the topical donors needed to be applied frequently, making the adherence to the treatment difficult. The electrospinning technique has allowed the production of a multilayer transdermal patch that produces a continuous and stable nitric oxide release. The main objective of this study is to evaluate this novel nitric oxide topical donor for the treatment of cutaneous leishmaniasis.
A double-blind, randomized, double-masked, placebo-controlled clinical trial, including 620 patients from endemic areas for leishmaniasis in Colombia was designed to investigate whether this patch is as effective as meglumine antimoniate for the treatment of cutaneous leishmaniasis but with less adverse events. Subjects with ulcers characteristic of cutaneous leishmaniasis will be medically evaluated and laboratory tests and parasitological confirmation performed. After checking the inclusion/exclusion criteria, the patients will be randomly assigned to one of two groups. During 20 days Group 1 will receive simultaneously meglumine antimoniate and placebo of nitric oxide patches while Group 2 will receive placebo of meglumine antimoniate and active nitric oxide patches. During the treatment visits, the medications will be administered daily and the presence of adverse events assessed. During the follow-up, the research group will visit the patients at days 21, 45, 90 and 180. The healing process of the ulcer, the health of the participants, recidivisms and/or reinfection will also be assessed. The evolution of the ulcers will be photographically registered. In the case that the effectiveness of the patches is demonstrated, a novel and safe therapeutic alternative for one of the most important public health problems in many countries will be available to patients.
| Condition | Intervention | Phase |
|---|---|---|
|
Cutaneous Leishmaniasis |
Drug: controlled nitric oxide releasing patch Drug: meglumine antimoniate |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Treatment |
| Official Title: | Double Blind, Randomized Controlled Trial, to Evaluate the Effectiveness of a Controlled Nitric Oxide Releasing Patch Versus Meglumine Antimoniate in the Treatment of Cutaneous Leishmaniasis |
- Complete reepithelization [ Time Frame: three months after the beginning of the treatment ] [ Designated as safety issue: No ]
- Absence of reactivation and affections of the mucous membranes [ Time Frame: during the first 6 months of the study ] [ Designated as safety issue: Yes ]
| Enrollment: | 178 |
| Study Start Date: | May 2006 |
| Study Completion Date: | March 2009 |
| Primary Completion Date: | January 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Active Comparator: 1 |
Drug: meglumine antimoniate
20mg/kg daily during 20 days
Other Name: glucantime
|
| Experimental: 2 |
Drug: controlled nitric oxide releasing patch
daily nitric oxide patch application during 20 days
|
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years to 50 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Men and women between 18 and 50 years old
- Cutaneous ulcers of more than two weeks of evolution
- Positive parasitological diagnosis for CL
- Patients that voluntarily agree to participate in the study and sign the informed consent.
- Disposition to attend all the visits punctually (initial, treatment and follow-up)
- Acceptation of not using any other treatment for CL while in the study
Exclusion Criteria:
- Pregnant women
- Presence of any condition or disease that compromises the patient immunologically (i.e. diabetes, cancer, etc.) or, any other, that, based on the judgment of the researcher, could alter the course of CL.
- Diffuse CL or more than five active lesions.
- Mucocutaneous leishmaniasis (no lesion must be located less than 2 cm from the nasal, uro-genital, and/or anal mucous membranes or from the edge of the lips).
- Visceral leishmaniasis
- Complete or incomplete treatment with antimony compounds in the last three months.
- Patients with history of hepatic, renal or cardiovascular disease.
- Mentally or neurologically disabled patients that are considered not fit to approve their participation in the study.
Contacts and Locations| Colombia | |
| Fundación Cardiovascular de Colombia | |
| Floridablanca, Santander, Colombia, 10000 | |
| Principal Investigator: | Patricio López-Jaramillo, MD, PhD | Cardiovascular Foundation of Colombia |
| Principal Investigator: | Daniel J Smith, PhD | Akron University |
| Study Chair: | Iván D Vélez, MD, MsC, PhD | Program for the Study and Control of Tropical Diseases, PECET, Universidad de Antioquia |
| Study Chair: | Gerardo Muñoz, PhD | Universidad Industrial de Santander |
| Study Chair: | Hernando Mosquera, MD | |
| Study Chair: | Federico A Silva, MD | Cardiovascular Foundation of Colombia |
| Study Chair: | Marcos López, PhD | The University of Akron |
| Principal Investigator: | Daniel Smith, PhD | The University of Akron |
| Study Chair: | Ligia C Rueda, MD | Fundación Cardiovascular de Colombia |
| Study Chair: | Christian F Rueda-Clausen, MD | Fundación Cardiovascular de Colombia |
More Information
No publications provided
| Responsible Party: | Victor Raúl Castillo Mantilla, Fundación Cardiovascular de Colombia |
| ClinicalTrials.gov Identifier: | NCT00317629 History of Changes |
| Other Study ID Numbers: | fcv137, 6566-04-18090 |
| Study First Received: | April 21, 2006 |
| Last Updated: | November 23, 2010 |
| Health Authority: | Colombia: INVIMA Instituto Nacional de Vigilancia de Medicamentos y Alimentos |
Keywords provided by Fundación Cardiovascular de Colombia:
|
leishmaniasis nitric oxide treatment donor controlled trial |
Additional relevant MeSH terms:
|
Leishmaniasis Leishmaniasis, Cutaneous Euglenozoa Infections Protozoan Infections Parasitic Diseases Skin Diseases, Parasitic Skin Diseases, Infectious Skin Diseases Nitric Oxide Meglumine antimoniate Bronchodilator Agents Autonomic Agents Peripheral Nervous System Agents Physiological Effects of Drugs Pharmacologic Actions |
Anti-Asthmatic Agents Respiratory System Agents Therapeutic Uses Free Radical Scavengers Antioxidants Molecular Mechanisms of Pharmacological Action Neurotransmitter Agents Endothelium-Dependent Relaxing Factors Vasodilator Agents Cardiovascular Agents Protective Agents Antiprotozoal Agents Antiparasitic Agents Anti-Infective Agents |
ClinicalTrials.gov processed this record on May 16, 2013