Fertility-female
Conditions
Interventions
Sponsors
Irshad Asma
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Infertile women with hyperprolactinemia confirmed by measuring fasting serum prolactin levels. 2. Women who give informed consent to participate in the study. 3. Women who are motivated to comply with study requirements including clinic visits, repeated blood sampling, vaginal drug administration and timely use of medication.
Exclusion criteria
Exclusion criteria: 1. Women with space occupying lesions or other complications requiring urgent intervention. 2. Women with active genital tract infections or cancers. 3. Renal or hepatic insufficiency. 4. Women who were already on treatment at the time of the study. 5. Women who were unable to provide informed consent. 6. Women with allergies to any component of the drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Percentage fall in serum prolactin levels during treatment in both arms of the study. 2.Proportion of women who experience side-effects in both arms of the study. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Proportion of women in both arms who achieve symptom relief following treatment. | — |
Countries
Nigeria
Contacts
Public ContactAliyu Sokomba
Senior Resident Ahmadu Bello University Teaching Hospital
Outcome results
None listed