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Human Papilloma Virus Infection clinical trials

View clinical trials related to Human Papilloma Virus Infection.

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NCT ID: NCT02124252 Completed - Clinical trials for Human Papilloma Virus Infection

Community-Driven Cervical Cancer Prevention in Western Kenya

Start date: January 2016
Phase: N/A
Study type: Interventional

There are many challenges to implementation of cervical cancer prevention in resource-limited countries, despite evidence based screening and treatment strategies. The investigators hypothesize that self-collected HPV specimens offered in a community health campaign setting will

NCT ID: NCT02067507 Completed - Clinical trials for Human Papilloma Virus Infection

Increasing Human Papillomavirus Vaccine Uptake in Low-Income, Ethnic Minority Adolescents in Los Angeles County

Start date: June 2012
Phase: N/A
Study type: Interventional

The primary aim of the project is to increase human papillomavirus (HPV) vaccine receipt rates among low-income, ethnic minority adolescents (girls and boys 11-17 years of age) in Los Angeles County. We will accomplish this goal by implementing and rigorously evaluating interventions in multiple venues that serve our target population, including the Los Angeles County Department of Public Health (LACDPH) and two large Federally Qualified Health Centers (FQHCs). Our hypotheses are: Primary hypothesis: 1. The intervention group will have a higher rate of HPV vaccine initiation at follow-up compared to the control group. Secondary hypothesis: 2. The intervention group will have higher vaccine completion rates (3 doses) at follow-up compared to the control group.

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: 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: 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.

NCT ID: NCT01898494 Active, not recruiting - Clinical trials for Stage III Squamous Cell Carcinoma of the Oropharynx

Transoral Surgery Followed By Low-Dose or Standard-Dose Radiation Therapy With or Without Chemotherapy in Treating Patients With HPV Positive Stage III-IVA Oropharyngeal Cancer

Start date: January 22, 2014
Phase: Phase 2
Study type: Interventional

This randomized phase II trial studies how well transoral surgery followed by low-dose or standard-dose radiation therapy works in treating patients with human papilloma virus (HPV) positive stage III-IVA oropharyngeal cancer. Radiation therapy uses high-energy x-rays to kill tumor cells. Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving radiation therapy with chemotherapy may kill any tumor cells that remain after surgery. It is not yet known how much extra treatment needs to be given after surgery.

NCT ID: NCT01567813 Completed - Clinical trials for Human Papilloma Virus Infection

Post-Licensure Study of the Safety of GARDASILâ„¢ in Males (V501-070)

Start date: June 23, 2011
Phase:
Study type: Observational

This is a post-licensure safety observation cohort study to describe the general safety of GARDASILâ„¢ (a quadrivalent human papillomavirus vaccine) in males.

NCT ID: NCT01539668 Completed - Prevention Clinical Trials

Hybrid Capture Test on Mobile Unit Program to Improve Cervical Cancer Screening in Brazilian Rural and Remote Areas

careHPV
Start date: March 2012
Phase: Phase 0
Study type: Observational

This study evaluates the women cervical samples through molecular tests in order to: 1. Deploy the test careHPV (hybrid capture test) in mobile unities of the Barretos Cancer Hospital to evaluate their performance;

NCT ID: NCT01446198 Completed - Clinical trials for Human Papilloma Virus Infection

Clinical Evaluation of the APTIMA® HPV Assay Using the PANTHERâ„¢ System

Start date: March 2012
Phase: N/A
Study type: Observational

The objective is to establish that APTIMA HPV Assay performance on the PANTHER System is comparable to performance on the TIGRIS System.

NCT ID: NCT01387997 Recruiting - Cervical Cancer Clinical Trials

e- Ab Sensor-based Real-time Detection of Oncogenic Human Papilloma Viruses

Start date: June 2010
Phase: N/A
Study type: Interventional

To develop a real-time diagnostic technique with e- Ab sensor for high risk human papilloma viruses(high risk HPV) detection, the investigators conduct a prospective clinical study. In comparison with results from direct sequencing of HPV, the investigators evaluate the performance of e- Ab sensor, including reproducibility, sensitivity, specificity, and cross-reaction (such as detection of low risk HPV). The potential factors which may interfere with the results would be investigated. With such a real-time diagnostic technique, the investigators hope to obtain information of patients in cost-saving and time-saving way and can give patients early treatment and offer more individualized treatment for our patients.