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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01233934
Other study ID # ERP 185v3-10
Secondary ID
Status Not yet recruiting
Phase Phase 3
First received November 2, 2010
Last updated November 2, 2010
Start date February 2011
Est. completion date July 2011

Study information

Verified date November 2010
Source Mantecorp Industria Quimica e Farmaceutica Ltd.
Contact Sergio Schalka, MD
Phone 551136811334
Email medci004@terra.com.br
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

Insect bite related symptoms (pruritus and papules) are caused by the release of histamine by mast cells in the skin. Topical anti-histaminics can be used to promote relief of these symptoms. Dexchlorpheniramine maleate 1% cream is a topical anti-histaminic formulation approved by ANVISA in Brazil for the relief of skin irritation and allergies, including the ones caused by insect bites. The aim of the present study is to demonstrate non-inferiority of a new pharmacological preparation of dexchlorpheniramine maleate (1% gel) with the standard preparation (1% cream) for the relief of insect bite related symptoms and to demonstrate the safety of both preparations.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 90
Est. completion date July 2011
Est. primary completion date July 2011
Accepts healthy volunteers No
Gender Both
Age group 2 Years to 60 Years
Eligibility Inclusion Criteria:

- Presence of papules resulting from insect bites within the last 72 hours;

- Presence of symmetric lesions to compare one side to the other;

- Compliance of the subject to the treatment protocol;

- Agreement with the terms of the informed consent by the participants or their legal guardians when younger than 18 years old.

Exclusion Criteria:

- Pregnancy or risk of pregnancy;

- Lactation;

- Use of topical or systemic anti-inflammatory, anti-histaminics or immunosuppressive drugs within the last 48 hours prior to the study;

- History of atopy or allergic diseases;

- History of allergy of any component of the formulations;

- Other conditions considered by the investigator as reasonable for non-eligibility.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Dexchlorpheniramine 1% Gel
Small amount applied over the lesion twice a day for 7 days.
Dexchlorpheniramine 1% Cream
Small amount applied over the lesion twice a day for 7 days.

Locations

Country Name City State
Brazil Medcin Instituto da Pele Ltda. Osasco São Paulo

Sponsors (1)

Lead Sponsor Collaborator
Mantecorp Industria Quimica e Farmaceutica Ltd.

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pruritus Intensity at Insect Bite Site, Evaluated With a 10 Point Visual Analogic Scale (VAS) 7 days No
Secondary Composite Clinical Evaluation of Erythema, Pruritus and Papule Formation, Performed by the Investigator Using a 4-point Scale for Each One of the Parameters (Absent, Mild, Moderate, Intense). This Evaluation Constitutes the Insect Bite Score. 7 days No
See also
  Status Clinical Trial Phase
Completed NCT03999970 - A Clinical Study to Develop an Uninfected Sand Fly Biting Protocol N/A
Completed NCT04512742 - A Clinical Study to Develop a Controlled Human Infection Model Using Leishmania Major-infected Sand Flies N/A
Active, not recruiting NCT00825214 - Evaluation of Zapperclick Device for Relief From Mosquito Bites Phase 3
Terminated NCT03619746 - Point-of-Care Ultrasound Educational Initiative for Insect Bites N/A
Unknown status NCT00995397 - Non-inferiority Clinical Trial of Dexchlorpheniramine (Cream Versus Lotion) in the Relief of Insect Bite Related Symptoms Phase 3