Status:

UNKNOWN

Efficacy of an Intravaginal Treatment With Carboxymethyl-β-glucan and Polycarbophil in HR-HPV Clearance

Lead Sponsor:

Uriach Consumer Healthcare

Collaborating Sponsors:

Hospital Universitario Infanta Leonor

Conditions:

Human Papilloma Virus

Eligibility:

FEMALE

30-40 years

Phase:

NA

Brief Summary

These treatments are beta-glucans, polysaccharides of beta-D-glucose that, can influence the clearance of HPV infection. The objective of this study is to evaluate the efficacy of a gel with Carboxyme...

Detailed Description

Background Human papillomavirus (HPV) infection represents a significant source of morbidity and mortality worldwide. High-risk oncogenic HPVs cause 99.7% of cervical cancers. 80% of sexually active ...

Eligibility Criteria

Inclusion

  • Sexually active women
  • between 30 and 40 years old
  • HR-HPV+ test (genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66 and 68)
  • normal cytology

Exclusion

  • Current or previous pregnancy ended before six weeks in relation to the start of the study.
  • Vaccination against HPV.
  • Clinically relevant pathology linked to immunodeficiency.
  • Immunosuppressive treatment active or finished before six months in relation to the start of the study. In the specific case of corticosteroids, all women who are receiving corticosteroid treatment currently or recently (defined as the two weeks prior to the start of the study) or if she has received 2 or more cycles of corticosteroids in equal or greater than 20 mg / day of predsinone (or equivalent) orally or parenterally, for one week duration at least in the year prior to the start of the study. The use of inhaled corticosteroids, Nasal or topical are not exclusion criteria.
  • Undiagnosed abnormal genital bleeding.
  • Total hysterectomy.
  • Presence of genital warts and other symptomatic vulvovaginal infections.
  • Documented history of cervical pathology caused by HPV.
  • Current systemic and / or gynecological disease that contraindicates the use of Colpofix.
  • Contraindications to the use of Colpofix or known allergies to any of its components
  • Simultaneous participating in a clinical study of an investigational drug or that could interfere with the use of Colpofix.

Key Trial Info

Start Date :

June 15 2021

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

September 1 2023

Estimated Enrollment :

200 Patients enrolled

Trial Details

Trial ID

NCT04781023

Start Date

June 15 2021

End Date

September 1 2023

Last Update

June 10 2021

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Hospital Universitario Infanta Leonor

Vallecas, Madrid, Spain, 28031