Clinical Trials Logo

Papilloma clinical trials

View clinical trials related to Papilloma.

Filter by:

NCT ID: NCT02634190 Completed - Clinical trials for Human Papilloma Virus Infection

Clinical Evaluation of the APTIMA® HPV Assay and Comparison With the HR HC2® Test Using LBC ThinPrep® Specimens

Start date: June 2009
Phase:
Study type: Observational

To assess and compare the performance of the HR HPV HC2® test (Qiagen/Digene) and the APTIMA® HPV Assay (Hologic) using LBC Specimens (ThinPrep® Pap Test) for the detection of HPV infection and high-grade CIN lesions in a screening population of women 30 years of age or older in Germany.

NCT ID: NCT02632344 Active, not recruiting - Clinical trials for Recurrent Respiratory Papillomatosis

Pembrolizumab for HPV-associated Recurrent Respiratory Papilloma Patients

Start date: April 2016
Phase: Phase 2
Study type: Interventional

This research study is evaluating an immune modulatory agent as a possible treatment for patients with Recurrent Respiratory Papillomatosis (RRP) with significant disease involving the larynx, trachea, and/or lungs. The investigators will be using Pembrolizumab as the treating agent.

NCT ID: NCT02624349 Completed - Clinical trials for Human Papillomavirus-Related Carcinoma

Immunogenicity and Safety of Human Papilloma Virus Vaccine in Solid Organ Transplant Recipients

Start date: October 2013
Phase: Phase 4
Study type: Interventional

The human papilloma virus (HPV) is known to be an important cause of cervical and anal cancers. Studies on patients who have received a solid organ transplant (such as a liver or kidney transplant) have suggested the risk of HPV-related cancers may be higher in this population. The HPV vaccine, Gardasil®, has been approved for use in males and females by Health Canada. In studies on healthy subjects this vaccine is nearly 100% effective at preventing infections from HPV serotypes that are in the vaccine. These serotypes, representing different viral strains, are known to cause 70% of cervical cancers and 90% of genital warts. The vaccine was also shown to be very safe and well tolerated in healthy subjects. Transplant patients are at higher risk of HPV related complications and cancers. As a result transplant experts have recommended this vaccine for use in their patients; however there have been no studies looking at the response to vaccination or safety of this vaccine in solid organ transplant recipients. Our objective is to study the immune response and side effects of Gardasil® in children who have received kidney or liver transplants. We will study this by comparing immune responses to the vaccine in healthy adolescent females compared to female liver and kidney transplant recipients. We will be recruiting females ages 12-19, as the province of Ontario funds the vaccine for this group. We will evaluate the transplant subjects for side effects after they receive the vaccine. Our hypothesis is that transplant recipients will have lower immunogenicity than healthy controls.

NCT ID: NCT02592902 Completed - Clinical trials for Recurrent Respiratory Papillomatosis

Recurrent Respiratory Papillomatosis and Extraesophageal Reflux

Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of the study was to determine, whether patients with recurrent respiratory papillomatosis (RRP) suffer from extra oesophageal reflux more often than patients with laryngeal cyst (control group).

NCT ID: NCT02576054 Completed - Condyloma Acuminata Clinical Trials

Safety and Tolerability Study of V501 in Japanese Boys (V501-200)

Start date: November 20, 2015
Phase: Phase 3
Study type: Interventional

This is a study of V501 [quadrivalent Human Papillomavirus (HPV) (Type 6, 11, 16 and 18) L1 virus-like particle (VLP) vaccine] in healthy Japanese boys. This study will consist of two periods. Period I of the study is to evaluate the immunogenicity and tolerability of V501 up to Month 7. Period II of the study is to evaluate the long-term immunogenicity and safety from Month 7 to Month 30. Two analyses are planned. The first analysis will be conducted when all subjects have completed their Month 7 visit or have been discontinued before that time. The second analysis will be conducted at the end of study. The primary hypothesis tested in this study is that seroconversion rates for the vaccine HPV types will be >90% at 4 weeks postdose 3.

NCT ID: NCT02558803 Completed - Cervical Cancer Clinical Trials

HPV Vaccination: Evaluation of Reminder Prompts for Doses 2 & 3

Start date: February 2015
Phase: N/A
Study type: Interventional

Randomized, 2-arm observational study. The 2 arms (randomized at the level of health care provider) will be: 1. usual practice; 2. automated reminders to recommend 2nd and 3rd doses of HPV vaccine for eligible male and female adolescents who have initiated vaccination.

NCT ID: NCT02555800 Recruiting - Clinical trials for Recurrent Respiratory Papillomatosis

Bevacizumab Versus Cidofovir for the Treatment of Recurrent Respiratory Papillomatosis

Start date: December 2014
Phase: Phase 2
Study type: Interventional

The aim of this study is to compare the efficacy of intralesional bevacizumab, a monoclonal antibody against vascular endothelial growth factor, versus the antiviral drug cidofovir in patients with recurrent respiratory papillomatosis.

NCT ID: NCT02551887 Completed - Cervical Cancer Clinical Trials

HPV Vaccination: An Investigation of Physician Reminders and Recommendation Scripts

Start date: February 2014
Phase: N/A
Study type: Interventional

Primary, Secondary, and Exploratory Objective(s): Primary objective: To evaluate the effect of interventions on 1st dose uptake of HPV vaccine.

NCT ID: NCT02546752 Completed - Cervical Cancer Clinical Trials

Use of a Patient Education/Messaging Platform to Increase Uptake and Series Completion of the HPV Vaccine

Start date: September 2015
Phase: Phase 0
Study type: Interventional

This primary goal of this study is to assess whether patient whose parents watch a standardized digital video using the integrated digital approach during a routine office visit are more likely to accept a dose of HPV vaccine (1st, 2nd, or 3rd dose) compared to those not completing the program. The study team anticipates eligible patients in the intervention clinics to have higher rates of HPV vaccine acceptance (1st, 2nd, or 3rd doses) than patients in the usual care comparison clinics. Additionally, the study team is interested in determining the impact of the integrated system on clinical workflow by measuring the number of minutes of each patient office visit when using the system compared to the number of minutes of each visit in offices where the system is not used. Although this is a descriptive/exploratory aim, our expectation is that the THEO system will have minimal impact on patient flow.

NCT ID: NCT02508701 Terminated - Clinical trials for Human Papilloma Virus, Male

A Pilot Study Comparing the Effectiveness of Campus Intervention to Increase HPV Vaccine Rate Among College Aged Men

Start date: August 2015
Phase: N/A
Study type: Interventional

This is a study testing what type of message and access influences a young male to get the HPV vaccine. The investigators are conducting a 2 X 2 design These conditions are: - Condition 1: Altruistic personal with direct recommendation inside-dorm - Condition 2: Generic message with inside-dorm - Condition 3: Generic message with outside-dorm HPV vaccine - Condition 4: Altruistic personal with outside-dorm HPV vaccine The objectives of this study are: A. To examine the efficacy in encouraging young men to receive HPV shots at Time 1 within each of the four intervention conditions (altruistic/personal with direct recommendation vs. generic message) X (in-dorm vs. outside-dorm HPV vaccine). B. To examine the efficacy in encouraging young men to receive HPV shots at Times 2 & 3 within each of the four intervention conditions (altruistic/personal with direct recommendation vs. generic message) X (in-dorm vs. outside-dorm HPV vaccine). 2.1.1 List the clinical hypotheses. Objective A H A.1: At Time 1, college men who have immediate access to the HPV vaccination will take the vaccination at a higher rate than those who do not have immediate access to the vaccine. H A.2: At Time 1, college men who receive an altruistic/personal health message along with immediate access to the HPV vaccine will take the HPV vaccination at a higher rate than the men in the other three arms of the study. Objective B H B.1: At Times 2 & 3, college men who have immediate access to the HPV vaccination will take the vaccination at a higher rate than those who do not have immediate access to the vaccine. H B.2: At Times 2 & 3, college men who receive an altruistic/personal health message along with immediate access to the HPV vaccine will take the HPV vaccination at a higher rate than the men in the other three arms of the study.