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IRB NUMBER: 202113087 IRB APPROVAL DATE: 06/02/2022Protocol: Longterm Human Papillomavirus Effectiveness and Immunity in Rwandan Women Living With and Without Human Immunodeficiency Virus NCT05247853
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01
Gather necessary personal information including name, date of birth, and contact details.
02
Provide medical history related to HPV, including any previous diagnoses or treatments.
03
Record vaccination status regarding HPV vaccines received.
04
Include details of any previous pap smears or HPV tests.
05
Fill out information about sexual history, including number of partners and any known STIs.
06
Complete the consent section, acknowledging understanding of the protocol and its purpose.
07
Review the completed protocol for accuracy before submission.

Who needs protocol long-term human papillomavirus?

01
Individuals who are diagnosed with HPV.
02
Patients who are undergoing regular monitoring for HPV-related conditions.
03
Adults considering HPV vaccination.
04
Healthcare providers managing HPV-related health care.
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Protocol long-term human papillomavirus refers to the systematic guidelines and procedures for monitoring and managing HPV infections over an extended period to assess their impact on health outcomes.
Healthcare providers, researchers, and organizations involved in HPV-related studies or public health initiatives are typically required to file for protocol long-term human papillomavirus.
Filling out the protocol involves providing detailed information on study objectives, designing data collection methods, ensuring ethical guidelines are followed, and outlining participant consent procedures.
The purpose is to establish a standardized approach for researching HPV's long-term effects, improving prevention strategies, and informing treatment options.
Information that must be reported includes participant demographics, HPV types, follow-up duration, health outcomes, methodologies used, and any adverse effects observed during the study.
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