GIOVANI DONNE TRA 18 E 35 ANNI MedDRA version: 9.1 Level: SOC Classification code 10036585 Term: Pregnancy, puerperium and perinatal conditions
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Sexually active women, to risk of pregnancy, that doesn't program luso of the condom; . Women that desire to make contraception and that they want to use an oral conraceptive for at least 6 months (6 cycles); . Age' inclusive among the 18 and the 35 years during the screening; . BMI understood among 17 and 35; . Physical and mental good state of health; . Women that accept a payment conraceptive; Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range
Exclusion criteria
Exclusion criteria: Side effect allassunzione of steroidi to contraceptive purpose: . Presence or history of events arterial or venous (for example deep venous thrombosis, pulmonary embolism, heart attack miocardico) trombotici / tromboembolici or of my goodness cerebrovascolari; . Presence or history of prodromi of thrombosis (for example attacks transitory ischemici, angina pectoris); . History of migraine with aura; . Diabetes type The and II
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: To appraise effect of three different contraceptive hormonal on the sensibility' insulinica in a group of women of age' inclusive between the 18 and the 35 years;Secondary Objective: To appraise effect of three different contraceptive hormonal on Body Mass Index (BMI), profile lipidico, functionality' liver in a group of women of age' inclusive between the 18 and the 35 years;Primary end point(s): To appraise effect of three different contraceptive hormonal on the sensibility' insulinica in a group of women of age' inclusive between the 18 and the 35 years | — |
Countries
Italy