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Papillomavirus Infections clinical trials

View clinical trials related to Papillomavirus Infections.

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NCT ID: NCT02048020 Completed - Clinical trials for Stage IV Squamous Cell Carcinoma of the Hypopharynx

Paclitaxel and Carboplatin Before Radiation Therapy With Paclitaxel in Treating HPV-Positive Patients With Stage III-IV Oropharynx, Hypopharynx, or Larynx Cancer

Start date: December 26, 2013
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well paclitaxel and carboplatin before radiation therapy with paclitaxel works in treating human papillomavirus (HPV)-positive patients with stage III-IV oropharynx, hypopharynx, or larynx cancer. Drugs used in chemotherapy, such as paclitaxel and carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high energy x rays to kill tumor cells. Giving paclitaxel and carboplatin before radiation therapy with paclitaxel may kill more tumor cells.

NCT ID: NCT02045186 Terminated - Clinical trials for Head and Neck Neoplasms

Monitoring of Oral Human Papillomavirus Infection (HPV) in HPV-positive Oropharyngeal Squamous Cell Carcinoma (OPSCC)

Start date: December 2013
Phase: N/A
Study type: Interventional

The purpose of this research study is to determine whether and when patients with human papilloma virus positive squamous cell cancer of the oropharynx treated with radiation and chemotherapy clear their human papilloma virus infection.

NCT ID: NCT02009800 Completed - Clinical trials for Human Papillomavirus Infections

ICI-VPH: Impact of HPV Immunisation Schedules Against HPV

ICI-VPH
Start date: November 2013
Phase: Phase 3
Study type: Interventional

This randomised clinical trial aims to determine whether an immunization schedule comprising two doses of Gardasil administered six months apart is non-inferior to a schedule comprising three doses administered at 0, 6 and 60 months for the prevention of HPV-16 and HPV-18 infections that persist for at least six months, up to ten years after the initial vaccination. The study hypothesis is that the two-dose schedule would offer similar protection as that of a three-dose schedule against persistent HPV-16/18 infections.

NCT ID: NCT02003508 Completed - Clinical trials for Human Papillomavirus

Prevalence of Genital HPV Infection in Males Following Introduction of Universal Male HPV Vaccination

Impress
Start date: January 2014
Phase:
Study type: Observational

This study will examine how common HPV infection is in teenage males in Australia before and after the introduction of universal school based vaccination of males in Australia.

NCT ID: NCT01995721 Not yet recruiting - Clinical trials for Recurrent Respiratory Papillomatosis

4-valent HPV Vaccine to Treat Recurrent Respiratory Papillomatosis in Children

Start date: February 2014
Phase: Phase 3
Study type: Interventional

Recurrent respiratory papillomatosis in children caused by HPV 6,11 can be a life threatening condition resulting in surgical interventions. The maturing and disintegrating papillomas are the sources for the subsequent HPV relapses and immunization might slow down or even prevent this ongoing process. After an initial immunological and ear-nose-throat (ENT) assessment children with at least 3 relapses in their patient history will be vaccinated with 4-valent HPV vaccine according to the following schedule: 0., 2., 6. months. It will be followed by an immunological and 3 ENT examinations to assess response to vaccination.

NCT ID: NCT01984697 Completed - Clinical trials for Human Papillomavirus Infection

A Phase III Study of a 2-dose Regimen of a Multivalent Human Papillomavirus (HPV) Vaccine (V503), Administered to 9 to 14 Year-olds and Compared to Young Women, 16 to 26 Years Old (V503-010)

Start date: December 12, 2013
Phase: Phase 3
Study type: Interventional

This was a 37-month safety and immunogenicity study conducted in boys and girls 9 to 14 years of age and in young women 16 to 26 years of age. From this study, the goal was to establish that the investigational 2-dose regimens (0, 6 months and 0, 12 months) studied in boys and girls 9 to 14 years of age are generally safe and immunogenic, with an antibody response that is not inferior to that observed in young women 16 to 26 years of age who received the standard 3-dose regimen of V503 (i.e., the population and dose regimen used to establish V503 efficacy).

NCT ID: NCT01946139 Completed - HIV Infection Clinical Trials

Anal HPV Tests in Screening for Cell Changes in the Anus in Patients With HIV

Start date: December 4, 2013
Phase: N/A
Study type: Interventional

This clinical trial studies anal human papillomavirus (HPV) tests in screening for cell changes in the anus in patients with human immunodeficiency virus (HIV). Screening tests may help doctors find cancer cells early and plan better treatment for anal cancer. Completing multiple screening tests may help find the best method for detecting cell changes in the anus.

NCT ID: NCT01932697 Completed - Clinical trials for Human Papillomavirus Infection

Radiation Therapy and Docetaxel in Treating Patients With HPV-Related Oropharyngeal Cancer

Start date: September 4, 2013
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well radiation therapy and docetaxel work in treating patients with human papillomavirus (HPV)-related oropharyngeal cancer. Radiation therapy uses high-energy x-rays to kill tumor cells. Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving radiation therapy with docetaxel my kill more tumor cells.

NCT ID: NCT01924117 Completed - Clinical trials for Intraepithelial Neoplasia

Genotypification and Predisposing Factors in Human Papilloma Virus Infection

HPV
Start date: February 2011
Phase: N/A
Study type: Interventional

Objective: Determine the genotypes and risk factors associated with human papilloma virus infection in Mexican women. Methods: It was a cross-sectional study of women attended at the Materno-Perinatal Hospital "Mónica Pretelini" and the Medical Research Center (CICMED), who were asked to complete a risk factor questionnaire and submitted to colposcopy to identify SIL. Cervical swab samples were obtained to perform linear array HPV genotyping test (Roche®, Mannheim, Germany).

NCT ID: NCT01901770 Active, not recruiting - Healthy Clinical Trials

The Parents in Appalachia Receive Education Needed for Teen Project

PARENT
Start date: January 2012
Phase: N/A
Study type: Interventional

This clinical trial studies an educational intervention for parents and providers in increasing human papillomavirus (HPV) vaccination rates in younger girls in Ohio Appalachia. Educational interventions may be effective in increasing the number of participants whose daughters receive HPV vaccination.