Reversible Effects of Oral Contraceptive Removal on Serotonergic Neurotransmission

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexFemale
Age18-39
SponsorRigshospitalet, Denmark

About this trial

The goal of this study is to learn about potential reversible effects of combined oral contraceptive (COC) use on the serotonergic brain system. The main question it aims to answer is:

\- If COC discontinuation results in an increase in serotonin 4 receptor binding in caudate, putamen, and hippocampus measured with Positron Emission Tomography from baseline to follow-up ≥ week 8 after discontinuation.

The secondary question it aims to answer is:

\- Over what timeframe the serotonin 4 receptor binding is restored after COC discontinuation to the level previously seen in a group of premenopausal women who had not used hormonal contraception before.

Researchers will compare discontinuation with continuation of a 2nd generation COC containing 150 ug levonorgestrel and 30 microgram to see if COC discontinuation results in an increased serotonin 4 receptor level in the brain.

\-

Participants will:

* Be randomized to discontinue or continue their COC use for 1-52 weeks. * Undergo an investigational program including brain scans, biological sampling, and neuropsychological testing at baseline and at follow-up.

The study uses a group sequential design with two sequential analyses planned, including an interim analysis after 60% of the brain scans have been acquired, which will be used to decide the timing of the last 40% of the scans - this is performed to best determine when the recovery of the serotonin 4 receptor level occurs.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Healthy women (assigned female at birth) at 18-39 years of age

Currently using a second-generation combined oral contraceptive containing 150 ug levonorgestrel and 30 ug ethinylestradiol for at least 3 months

Disqualifiers

Current or previous neurological or psychiatric disease, severe somatic disease, or consumption of medical drugs (including psychoactive medication) likely to influence the test results

Non-fluent in Danish or pronounced visual or auditory impairments

Current or past learning disability

Pregnancy within the last year or previous pregnancy lasting into second or third trimester

Trial design

Design model

Parallel

Treatments tested in this trial

  • Discontinuation of 2nd generation combined oral contraceptive use

    Drug

    Discontinuation of 2nd generation combined oral contraceptive use

  • Continuation of 2nd generation combined oral contraceptive use

    Drug

    Continuation of 2nd generation combined oral contraceptive use

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Combined oral contraceptive continuation (COCc)Active comparator 1 intervention
Group B: Combined oral contraceptive discontinuation (COCd)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in global serotonin 4 receptor (5-HT4R) brain binding across caudate, putamen, and hippocampus

Serotonin 4 receptor (5-HT4R) brain binding is measured with positron emission tomography. Change in global 5-HT4R brain binding is estimated using a latent variable model with a latent variable pooling the change in log-transformed binding potentials from baseline to follow-up across caudate, putamen, and hippocampus after adjustment for change in injected tracer mass per kg body weight.

Time frame
1-52 weeks

Secondary outcomes

1

Change in total Verbal Affective Memory Test-24 (VAMT-24) score

Verbal Affective Memory task 24 (VAMT-24) total recall score is calculated as the average score across the immediate (0-24), short- (0-24), and long-term (0-24) recall with higher scores representing better performance.

Time frame
1-52 weeks
2

Difference in hippocampal activation during memory encoding

Hippocampal blood-oxygen-level-dependent (BOLD) activation during a memory encoding paradigm.

Time frame
1-52 weeks
3

Change in brain insulin sensitivity

Hypothalamic blood flow response to oral glucose, used as a proxy for brain insulin sensitivity.

Time frame
1-52 weeks
4

Change in hypothalamic blood-oxygen-level-dependent response to oral glucose

Hypothalamic blood-oxygen-level-dependent response to oral glucose.

Time frame
1-52 weeks

Other outcomes

1

Change in area under the curve of glucose during an oral glucose tolerance test (OGTT)

Change in area under the curve during OGTT for glucose from baseline to follow-up.

Time frame
1-52 weeks
2

Change in area under the curve of insulin during an oral glucose tolerance test (OGTT)

Change in area under the curve during OGTT for insulin from baseline to follow-up.

Time frame
1-52 weeks
3

Change in area under the curve of c-peptide during an oral glucose tolerance test (OGTT)

Change in area under the curve during OGTT for c-peptide from baseline to follow-up.

Time frame
1-52 weeks
4

Change in Hba1C

Change in Hba1C from baseline to follow-up

Time frame
1-52 weeks

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