CompletedNot Applicable

Progesterone Containing Contraceptive Methods on Endogenous Progesterone Level

Egypt80 participantsStarted 2021-03-30

Plain-language summary

The aim of this study is to assess the effect of different progesterone containing contraceptive methods on safety and endogenous progesterone level

Who can participate

Age range

20 Years – 35 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 80 healthy fertile females * 20-35 years * With normal menstrual history * Had at least one offspring after spontaneous pregnancy Exclusion Criteria: * Any disease affects uterus (uterine tumors fibroids, endometriosis, prolapse, or tuberculosis). * Ovarian tumors * submucous myoma * irregular menstrual cycle * past or family history of breast disease * Diabetic patients, * medication affecting reproductive or metabolic functions. * endometrial thickness \<7 mm on the secretory transformation day * history of spontaneous abortions * history of embryo transfer failure on over three occasions * Patients had cortisol medications * patients who received radiological treatment

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Assess the effect of different progesterone containing contraceptive methods on safety and endogenous progesterone level

Timeframe: Six mounths

Trial details

NCT IDNCT05742503

SponsorTanta University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2022-03-30

View on ClinicalTrials.gov More Progesterone trials