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Glizigen-Viudid-External Anogenital Warts in Children and Adolescents

Primary Purpose

External Anogenital Warts

Status
Completed
Phase
Phase 3
Locations
Cuba
Study Type
Interventional
Intervention
Glizigen + Viusid
Placebo
Sponsored by
Catalysis SL
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for External Anogenital Warts focused on measuring Dietary supplement, Anogenital warts, Viusid, Glizigen

Eligibility Criteria

10 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • No previous treatment for anogenital warts
  • Negative serology for HB and HIV.
  • Signed informed consent.

Exclusion Criteria:

  • Pregnancy
  • Treatment with steroids, immune-suppressors, immune-modulators or local or systemic antiviral drugs.
  • Hypersensitivity to Glizigen or Viusid:

Sites / Locations

  • Pediatric Hospital "Dr. Juan Manuel Márquez".

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Glizigen + Viusid

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Time to lesion regression
Excellent: Lesion regression before 2 weeks of treatment Good: Lesion regression between 2-5 weeks of treatment Poor: Lesion regression between 5-8 weeks of treatment Bad: No lesion regression after 8 weeks of treatment.

Secondary Outcome Measures

Occurrence of adverse effects within the 12 week treatment period
Reduction in the number of lesions
Excellent: Regression in more than 75% of lesions Good: Regression in 50-75% of lesions Poor: Regression in 25-50% of lesions Bad: Regression in less than 25% of lesions.
Lesion aspect
Excellent: Lesion regression Poor: Aspect changes from papilloma shaped to flat shaped lesion. Bad: No change in aspect or change from flat shaped to papilloma shaped lesion.

Full Information

First Posted
April 26, 2010
Last Updated
May 6, 2012
Sponsor
Catalysis SL
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1. Study Identification

Unique Protocol Identification Number
NCT01111344
Brief Title
Glizigen-Viudid-External Anogenital Warts in Children and Adolescents
Official Title
Efficacy of Glizigen-Viudid in the Treatment of External Anogenital Warts in Children and Adolescents.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2012
Overall Recruitment Status
Completed
Study Start Date
December 2010 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
September 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Catalysis SL

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is to assess the efficacy of Glizigen and Viusid administration in the treatment of external anogenital warts in children and adolescents. The duration of this double-blind placebo controlled phase 3 clinical trial will be 12 weeks. The estimated number of persons to be recruited and randomized for the study is 76. Variables to be assessed will be: time to disappearance of lesions, reduction of the number of lesions and change in the aspect of lesions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
External Anogenital Warts
Keywords
Dietary supplement, Anogenital warts, Viusid, Glizigen

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
76 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Glizigen + Viusid
Arm Type
Experimental
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
Glizigen + Viusid
Intervention Description
Glizigen (spray, 60 mL bottle with applicator): Dosage commensurate with surface (up to a maximum of 10 cm2) to be treated. From 3 to 5 ambulatory applications (One nebulization corresponds to 2 short pulses). 1 to 3.9 cm2 ______________3 daily applications 4 to 6.9 cm2 ______________4 daily applications 7 to 10 cm2 ______________5 daily applications Treatment will last from 5 days to 8 weeks according to clinical improvement. Viusid (Syrop, 500 mL flask): 12.5 ml every 8 hours for 12 weeks. Viusid syrop should be dissolved in water, fruit juice or milk before ingestion.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Placebo Glizipen (spray, 60 mL bottle with applicator): Dosage commensurate with surface (up to a maximum of 10 cm2) to be treated. From 3 to 5 ambulatory applications (One nebulization corresponds to 2 short pulses). 1 to 3.9 cm2 ______________3 daily applications 4 to 6.9 cm2 ______________4 daily applications 7 to 10 cm2 ______________5 daily applications Treatment will last from 5 days to 8 weeks according to clinical improvement. Placebo Viusid (Syrop, 500 mL flask): 12.5 ml every 8 hours for 12 weeks. Viusid syrop should be dissolved in water, fruit juice or milk before ingestion.
Primary Outcome Measure Information:
Title
Time to lesion regression
Description
Excellent: Lesion regression before 2 weeks of treatment Good: Lesion regression between 2-5 weeks of treatment Poor: Lesion regression between 5-8 weeks of treatment Bad: No lesion regression after 8 weeks of treatment.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Occurrence of adverse effects within the 12 week treatment period
Time Frame
12 weeks
Title
Reduction in the number of lesions
Description
Excellent: Regression in more than 75% of lesions Good: Regression in 50-75% of lesions Poor: Regression in 25-50% of lesions Bad: Regression in less than 25% of lesions.
Time Frame
12 weeks
Title
Lesion aspect
Description
Excellent: Lesion regression Poor: Aspect changes from papilloma shaped to flat shaped lesion. Bad: No change in aspect or change from flat shaped to papilloma shaped lesion.
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: No previous treatment for anogenital warts Negative serology for HB and HIV. Signed informed consent. Exclusion Criteria: Pregnancy Treatment with steroids, immune-suppressors, immune-modulators or local or systemic antiviral drugs. Hypersensitivity to Glizigen or Viusid:
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Edelisa Moredo Romo, MD
Organizational Affiliation
Pediatric Hospital "Dr. Juan Manuel Márquez.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pediatric Hospital "Dr. Juan Manuel Márquez".
City
Havana
ZIP/Postal Code
10400
Country
Cuba

12. IPD Sharing Statement

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Glizigen-Viudid-External Anogenital Warts in Children and Adolescents

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