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Efficacy of the Glicigen – Viusid in the treatment of external genitals anus wart in children

CLINICAL TRIAL PHASE III "Efficacy of the Glicigen – Viusid in the treatment of external genitals anus wart in children"

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
RPCEC
Registry ID
RPCEC00000097
Enrollment
Unknown
Registered
2010-09-04
Start date
2010-09-06
Completion date
Unknown
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

external anus genitals wart

Interventions

Group A: Glicigen+Viusid Glicigen: For 3 to 5 daily application (dependent of the lesion skin size) beetewn 5 days to 8 weeks according to the clinical evolution. There will be topical application (sp

Sponsors

Catálysis S.L.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 18 Years

Inclusion criteria

Inclusion criteria: Patient with lesions characteristic and diagnostic of (externalanus genitals warts) To be included beetwen 6 and 18 years old of both sexes.(Identify Card) Signed informed consent Negative VDRL, Hepatitis B Antigen and HIV diagnostic test

Exclusion criteria

Exclusion criteria: With previous treatment Pregnant Patients taking steroides, inmunomodulates and topic and sistemic antivirals therapy Patient that refer manifestations of high sensibility to the medication

Design outcomes

Primary

MeasureTime frame
Disappearance of the lesions (Excellent, Good, Regular, Bad). Measurement time: 2, 4, 6,and 8 weeks after treatment. Excellent (E): Disappearance of the lesions in less than 2 Weeks of initiated the treatment Good (B): Disappearance of the lesions between 2 and 5 weeks of initiated the treatment Regular (R): Disappearance of the lesions between 6 and 8 weeks of initiated the treatment Bad (M) Not Disappearance of the lesions after 8 weeks of treatment.

Secondary

MeasureTime frame
Reduction of the number of the lesions (Excellent, Good, Regular, Bad).Measurement time: 8 weeks after treatment. Excellent (E) Disappearance of the lesions or reduction equal or more than 75 % Good (B) Reduction between 50 % and less than 75% Regular (R): Reduction less than less than 50 % and more than 25% Bad (M): Reduction equal or less than 25% Appearance of the lesion (flats, papilomatouse): (Good, Regular, Bad). Measurement time: 8 weeks after treatment. Good. Disappearance of the lesion Regular: Changes the appearance from papilomatouse to flat Bad: When remains the same appearance or changes to papilomatouse Adverse lesions present during treatment (good, Regular, Bad). Measurement time: 8 weeks after treatment. Good: Not presents adverse lesions during treatment Regular: Presents adverse lesions but, is possible to continue the treatment Bad: Presents adverse lesions and Is not possible to continue the treatment

Countries

Cuba

Contacts

Public ContactEdelisa Moredo

Juan Manuel Márquez Pediatric Educational Hospital

edelisa.moredo@infomed.sld.cu

Outcome results

None listed

Source: RPCEC (via WHO ICTRP) · Data processed: Aug 15, 2026