Hypertension
Conditions
Interventions
This is a single arm clinical trial in which forty women will receive a combined oral contraceptive containing nomegestrol acetate with estradiol and will be evaluated before and after use using labor
Sponsors
Universidade de Gurupi
Universidade de Gurupi
Eligibility
Sex/Gender
Female
Age
18 Years to 49 Years
Inclusion criteria
Inclusion criteria: Women of reproductive age; over 18 years old; classified as class 1 or 2 according to WHO eligibility criteria
Exclusion criteria
Exclusion criteria: Women under 18 years of age or postmenopausal; with absolute or relative contraindications to the use of estrogens
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find that blood pressure levels and glycemic and lipid profiles as well as anthropometric measurements will remain stable | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected that modifying factors will have an influence, such as level of physical activity (IPAQ); smoking and alcohol consumption; adherence to the contraceptive method;It is expected that participants will experience a high degree of satisfaction with the contraceptive method and a desire to continue using it after 6 and 12 months | — |
Countries
BR
Contacts
Public ContactFabiana Anjos
Universidade de Gurupi- UNIRG
Outcome results
None listed