Genital warts. Anogenital (venereal) warts
Conditions
Interventions
Intervention 1: Intervention group 1: gel containing green tea extract and pecan seeds in a 50-50 ratio. Intervention 2: Control group: gel containing green tea extract. Intervention 3: Intervention g
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: The individual must not have any specific medical illnesses. They should have no other sexually transmitted diseases (STDs) In the past 6 months, they should not have been under psychiatric supervision and should not be taking psychiatric medications. They must not be allergic to green tea or pennyroyal seeds They should not have speech or behavioral disorders that hinder communication with the researcher. They must not have genital warts inside the vagina Genital warts should be limited to the skin. The number of lesions should be between 2 and 30 The surface area of lesions should be between 2 and 600 square millimeters Their spouse should not have genital warts They should have no history of using specific medications. Both they and their spouse should have only one sexual partner.
Exclusion criteria
Exclusion criteria: They are breastfeeding or pregnant. They are smoker They are infected with other STDs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number and size of external genital wart lesions. Timepoint: Every two weeks until the 10th week. Method of measurement: The patient is examined by the researcher and all areas of the genital area such as the posterior foreskin, labia majora, groin, pubic and anal areas, and perianal are examined for the presence of lesions and the number and size of the lesions are recorded. To determine the initial size of the lesion, the two main perpendicular diameters of each lesion are measured in millimeters with a ruler and the area of ??each lesion is obtained from the product of these two diameters. | — |
Secondary
| Measure | Time frame |
|---|---|
| Occurrence of new lesions. Timepoint: Every two weeks. Method of measurement: Observation.;Occurrence of reactions and side effects. Timepoint: Every two weeks. Method of measurement: Questioning the patient. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDavoud Salarbashi
Gonabad University of Medical Sciences
Outcome results
None listed