Effectivity of Protein Purified Derivative Treatment for Anogenital Warts in HIV Patient
NCT ID: NCT06587542
Last Updated: 2024-09-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
PHASE2/PHASE3
30 participants
INTERVENTIONAL
2024-09-15
2025-12-31
Brief Summary
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Detailed Description
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Data, Data Collection Techniques and Data Sources The data used is primary data. Primary data is the result of examination anogenital warts patients who were then given PP2-TU therapy at varying doses, blood serum and histopathological preparations are taken before injection and 3 weeks after the injection.
Sample Taking/Selection The research sample was anogenital warts patients who were treated at the Infection Polyclinic Sexually Transmitted Hospital Dr. Hasan Sadikin Bandung, using consecutive sampling for each group, 15 anogenital warts patients with and 15 patient without HIV infection were given purified protein derivative injection.
Data Validity and Reliability The validity of laboratory examination data can be guaranteed due to inspection. Laboratory work is carried out in the clinical pathology and anatomical pathology laboratories of the Hospital Dr Hasan Sadikin who has international standards.
Independent variable: Patients with anogenital warts Dependent variables: Clinical response, levels of IFN-α, IFN-γ, and IL-2 in the blood and tissue.
Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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HIV-positive patients with anogenital warts
Injection of protein purified derivative
Injection of protein purified derivative
Injection of purified protein derivative for anogenital warts in HIV and non HIV patient, on the largest lesion
HIV-negative patients with anogenital warts
Injection of protein purified derivative
Injection of purified protein derivative for anogenital warts in HIV and non HIV patient, on the largest lesion
Interventions
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Injection of protein purified derivative
Injection of purified protein derivative for anogenital warts in HIV and non HIV patient, on the largest lesion
Eligibility Criteria
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Inclusion Criteria
2. All stored biological materials that have been previously taken through tissue from anogenital warts patients whose diagnosis was confirmed based on history and physical examination, 3 weeks after receiving the first intralesional purified protein derivative injection therapy.
Exclusion Criteria
3\. Have an immunodeficiency disease based on anamnesis and clinical examination, except for HIV based on anamnesis, clinical examination and serological examination (anti-HIV).
4\. Have a history of suffering from malignancy based on history and clinical examination.
5\. Infected with tuberculosis based on history, clinical examination and chest radiography.
6\. Infected with other STIs based on history, clinical examination, and serological examination (venereal disease research laboratory (VDRL), Treponema pallidum hemagglutination assay (TPHA), and Hepatitis B surface antigen (HBsAg)).
15 Years
60 Years
ALL
No
Sponsors
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Universitas Padjadjaran
OTHER
Responsible Party
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Central Contacts
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References
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Achdiat PA, Widjaja S, Suwarsa O, Dwiyana RF, Hindritiani R, Sutedja E, Gunawan H, Usman HA, Rianty F, Maharani RH. Effectiveness and safety of tuberculin purified protein derivative for the treatment of anogenital warts in patients with human immunodeficiency virus. Dermatol Reports. 2024 Jan 30;16(3):9754. doi: 10.4081/dr.2024.9754. eCollection 2024 Sep 2.
Other Identifiers
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DV-202407.01
Identifier Type: -
Identifier Source: org_study_id
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