Birth control pill withdrawal: how long until hormones normalize?
NCT ID NCT06802211
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how long it takes for a key stress hormone (cortisol) and its carrier protein to return to normal after healthy women stop taking combined oral contraceptive pills. Twenty-four women were followed for several weeks after stopping the pill. The goal was to understand the timing of hormone recovery, which can help doctors interpret lab results and guide care.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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24 people
The number who actually took part.
- Started
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Feb 2025
- Finished
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Nov 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult females who are planning to discontinue estrogen containing oral contraceptives for a duration of at least 6 weeks.
- Ages
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18 years and older
- Sex
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Female participants only
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * ≥18 years old * Using oral combined contraceptives of any kind and dosage * Planning to stop COC use shortly for at least 6 weeks (out of own reasons such as a pregnancy wish or choice for non-hormone based contraceptives) * COC use for at least 3 consecutive weeks before the discontinuation * Ability to provide informed consent * Ability to speak and understand Dutch Exclusion Criteria: * Switching to other hormonal contraceptives after taking the COC pill (e.g. progesterone containing contraceptives such as the Mirena IUD, contraceptive implants) directly after the discontinuations * Contra-indications to quit COC * Biological factors that affect CBG concentrations, including: * Illnesses interfering with CBG levels (severe liver or kidney disease, active malignancy, hyperthyroidism) * Use of insulin, systemic exogenous glucocorticoids, mitotane, selective estrogen receptor modulators (SERMs) * Pregnancy during study period after discontinuation of COCs
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Amsterdam UMC
Amsterdam, 1105 AZ, Netherlands