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AzTrials

ScizophreniaPhase 4NCT07386080

Carbergoline for Antipsychotic Induced Hyperprolactinemia.

A Phase 4 study testing Cabergoline (Dopamine Agonist) in people with Scizophrenia, run by Zealand University Hospital at 1 site in Denmark.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The goal of this clinical trial is to learn if cabergoline is safe to use in patients with antipsychotic-induced hyperprolactinemia in adults with scizophrenia. The main question it aims to answer : Is the severity of positive and negative symptoms affected by the use of cabergoline? Researchers will compare… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Scizophrenia
What is being tested?
Cabergoline (Dopamine Agonist)
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
146 participants
Where
1 siteDenmark
Study dates
1 May 2026to 1 May 2029
Phase
Phase 4
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • receiveing antipsychotic treatment for at least 3 months for a schizophrenia spectrum disorder
  • Prolactin levels > URL
  • symptoms of hyperprolactinemia according to he UKU side effect scale (Udvalg for Klinisk Undersøgelser)
  • no suicide ideation at time of recruitment (≤ 2 Columbia-Suicide Serverity Rating Scale)

Who cannot join

  • patients that has previously responded unfavorably to treatment with a dopamine receptor agonist.
  • The use of recreational drugs that may give hyperprolactinemia.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Jesper Krogh, MD, PhD. contact

+45 25535485

jekrog@regionsjaelland.dk

Denmark1 site
  • Zealand University Hospital

    Køge, Region Sjælland, 4600

Other trials in Denmark

About this study

Official title: The Safety of Carbergoline Versus Placebo for Antipsychotic Induced Hyperprolactinemia: A Pragmatic, Randomised, Non-inferiority Trial With Blinded Outcome.

The goal of this clinical trial is to learn if cabergoline is safe to use in patients with antipsychotic-induced hyperprolactinemia in adults with scizophrenia. The main question it aims to answer :

Is the severity of positive and negative symptoms affected by the use of cabergoline?

Researchers will compare cabergolin to placebo to see if positive and negative symptoms are equel in both groups.

Participants will, in a blinded manor, take either placebo tablets or cabergoline for 12 weeks. The severity of positive and negative symptoms will be evaluated before and after the intervention in both groups.

Read the detailed description

Antipsychotic (AP) medication is the cornerstone of treatment in patients with schizophrenia, but may be used in patients with depression, severe anxiety, or bipolar disorders. The main regulator of prolactin is exerted by the inhibitory effect of hypothalamic dopamine through its agonistic effects on pituitary D2-receptors. The majority of antipsychotic drugs require a 50 to 60% antagonistic occupancy of the D2 receptor for optimal effect, which explains why hyperprolactinemia is observed in 30% to 70% of patients on AP treatment. Hyperprolactinemia may cause gynecomastia, galactorrhea, infertility, menstrual irregularities, osteopenia, sexual dysfunction, and erectile dysfunction in men, while metabolic and cardiovascular disturbances are currently debated5 - serious side effects that may contribute to the low adherence rates of antipsychotic treatment in patients with schizophrenia spectrum disorders. The consistent association between lack of adherence to treatment and hospitalisation, acute care utilization, and relapse prevention highlights the importance of safe antipsychotic treatment with acceptable side effects. Unacceptable side effects to AP treatment may incline patients and physicians to abandon otherwise successful AP treatment and pursue treatment with less potent antipsychotic properties but with fewer and acceptable side effects. Since 2015, the proportion of Danish citizens treated with antipsychotics has increased every year up to 144.000 in 2023, corresponding to an increase of 19% in less than a decade.

While the effect of prolactin on breast tissue is a direct result of prolactin binding to prolactin receptors the other symptoms of hyperprolactinemia are mainly indirect through reduced gonadotropin levels, i.e. estrogen and testosterone; high prolactin levels result in decreased kisspeptin in the hypothalamus and consequently gonadotropin-releasing hormone (GnRH) release is reduced which leads to lower secretion of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), which is then followed by lower levels of estradiol and testosterone. It could also be hypothesised that hyperprolactinemia may have unwarranted metabolic effects, as often observed in patients in antipsychotic treatment. Current strategies for reducing antipsychotic induced hyperprolactinemia include a change of AP treatment, aripiprazole, estrogen or testosterone supplementation, metformin, or a dopamine receptor agonist (DRA) - i.e. cabergoline or bromocriptine. Once effective APT has been established, changing or reducing the drug or dose is often not desirable, and only aripiprazole, metformin, and DRAs will address both direct and indirect effects of hyperprolactinemia. From an endocrine perspective, treatment with DRAs is tempting due to the fast and highly effective prolactin-lowering properties, the low prevalence of side effects, and administration once or twice weekly (cabergoline).

However, from a theoretical point DRA-treatment may be problematic due to the opposing effects of antipsychotics and DRAs on the dopamine receptor, which may cause exacerbations of psychotic symptoms, which is why endocrinologists are reluctant to introduce DRAs for AP-induced hyperprolactinemia. However, several observational studies have shown significant effect of DRAs on prolactin levels and symptoms associated with AP induced hyperprolactinemia without any adverse effects to psychopathological status, while one RCT found worsening of psychotic symptoms in 1/2018 comparing bromocriptine with a herbal product and only one RCT has examined bromocriptine versus placebo in 60 patients without identifying any worsening in psychopathology. None of the RCT's used blinded outcome assessment, and none of the studies used cabergoline, which is the dopamine receptor agonist with the least number of adverse events, and only requires administration once or twice weekly.

Main objective • Assessing the safety of cabergoline for antipsychotic induced hyperprolactinemia in men and pre-menopausal women with schizophrenia spectrum disorders concerning positive and negative symptoms in a randomised, parallel group, non-inferiority trial with blinded outcome assessment.

Main hypothesis

  • We hypothesise that the severity of positive and negative symptoms in participants with antipsychotic induced hyperprolactinemia receiving cabergoline is non-inferior to placebo after 12 weeks of intervention.

Perspective With the high prevalence of AP-induced hyperprolactinemia, the use of cabergoline for augmentation of both direct and indirect effects of high prolactin levels would offer patients an effective prolactin-lowering strategy, few side effects, and allow patients to stay on effective antipsychotic treatment. With a convincing and safe treatment for AP-induced hyperprolactinemia, we expect a larger proportion of patients to be able to remain on the best AP-treatment with no or reduced side-effects from hyperprolactinemia. With the addition of clear guidelines, the treating psychiatrist may, in the future, treat AP-induced hyperprolactinemia themselves rather than referring to an endocrinologist and risk treatment delay. Reducing prolactin levels with cabergoline may also contribute to an improved metabolic profile as observed in patients with type 2 diabetes or hyperprolactinemia.

Method Design: A pragmatic randomised controlled parallel group non-inferiority study with blinded outcome assessment.

Conditions
Scizophrenia
Being tested
Cabergoline (Dopamine Agonist), Placebo
Keywords
prolactin, cabergoline

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Cabergoline (Dopamine Agonist)Drug

    This intervention will use cabergoline for antipsychotic induced hyperprolactinemia.

  • PlaceboDrug

    Placebo + standard care

Study groups in NCT07386080
Study groupRoleWhat they receive
PlaceboPlacebo comparatorPlacebo tablets + standard care
Receives: Drug: Placebo
InterventionActive comparatorCabergoline tablets + standard care
Receives: Drug: Cabergoline (Dopamine Agonist)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Total score on the PANSS (Positive and Negative Syndrome Scale)

    The primary outcome is the total score of the PANSS in absolute numbers at the end of intervention (12 weeks) comparing the placebo group with the intervention group (cabergoline).

    Measured: At end of intervention, i.e. 12 weeks from baseline.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Feb 2026
  2. Study start1 May 2026 (estimated)
  3. Primary completion1 May 2028 (estimated)
  4. Study completion1 May 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
146 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07386080
Sponsor's protocol ID
JK-1002
Status last verified
Jan 2026
First submitted
27 Jan 2026
Last updated
4 Feb 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: IPD data will be shared upon reasonable request provided that a data sharing agreement can bee reached and that the local ethical committee will accept.

Publications

  • Kuroki T, Watanabe Y, Yamai S, Obara Y, Takizawa K. [Detection of Neisseria gonorrhoeae antigens by an enzyme immunoassay (Gonozyme)]. Kansenshogaku Zasshi. 1985 Dec;59(12):1236-40. doi: 10.11150/kansenshogakuzasshi1970.59.1236. No abstract available. Japanese.

    PubMed 3938800
  • Gonzalez-Rodriguez A, Labad J, Seeman MV. Antipsychotic-induced Hyperprolactinemia in aging populations: Prevalence, implications, prevention and management. Prog Neuropsychopharmacol Biol Psychiatry. 2020 Jul 13;101:109941. doi: 10.1016/j.pnpbp.2020.109941. Epub 2020 Mar 31.

    PubMed 32243999
  • Lang K, Meyers JL, Korn JR, Lee S, Sikirica M, Crivera C, Dirani R, Menzin J. Medication adherence and hospitalization among patients with schizophrenia treated with antipsychotics. Psychiatr Serv. 2010 Dec;61(12):1239-47. doi: 10.1176/ps.2010.61.12.1239.

    PubMed 21123409

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Cabergoline (Dopamine Agonist) in people with Scizophrenia, run by Zealand University Hospital at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 4 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Jesper Krogh, MD, PhD. (+45 25535485, jekrog@regionsjaelland.dk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Total score on the PANSS (Positive and Negative Syndrome Scale) (time frame: At end of intervention, i.e. 12 weeks from baseline.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07386080, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Feb 2026.

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