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UnknownNCT00315081

Risperidone-Induced Hyperprolactinemia Treated With Bromocriptine

Therapy With Bromocriptine in Patients With Symptomatic Risperidone-Induced Hyperprolactinemia

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
20 (planned)
Sponsor
University Hospital, Bonn · Academic / Other
Sex
Male
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Antipsychotic drugs can cause a clinically relevant hyperprolactinemia due to blocking the dopamine receptors in the pituitary.Schizophrenic patients suffering from a neuroleptic-induced hyperprolactinemia will be examined endocrinologically. Adverse drug effects and diagnoses will be confirmed by measuring hormones.

Detailed description

Antipsychotic drugs can cause a clinically relevant hyperprolactinemia due to blocking the dopamine receptors in the pituitary.Depending on its concentration hyperprolactinemia causes a median hypogonadism with estrogen insufficiency in women and testosterone insufficiency in men by inhibiting the pulsatile GnRH-secretion.The hyperprolactinemia-induced symptoms have been successfully medicated for years with dopamine agonists like bromocriptine. In patients with psychiatric diseases hyperprolactinemia is usually not treated with dopamine agonist fearing a reexacerbation of the underline psychiatric disease. In a few studies and casuistically the treatment of neuroleptic-induced hyperprolactinemia with bromocriptine has been shown to be effective without causing reexacerbation of psychotic symptoms. Schizophrenic patients suffering from a neuroleptic-induced hyperprolactinemia (in extremis galactorrhoea and amenorrhoea. in women, loss of libido and erectile dysfunction in men) will be examined endocrinologically. Adverse drug effects and diagnoses will be confirmed by measuring hormones (prolactin, LH, FSH, testosterone, estradiol). In case of a clear symptomatic, neuroleptic-induced hyperprolactinemia patients will be medicated with bromocriptin. Therapeutical success will be determined endocrinologically in week 0, 1, 2, 3, 4, 8, 12, 16, 20 and 24 together with a psychiatric examination (PANSS, HAM-D, Simpson-Angus Scale (SAS)). Safety of therapy will be ensured by the close meshed psychiatric examinations.

Conditions

Interventions

TypeNameDescription
DRUGBromocriptin

Timeline

Start date
2006-05-01
Completion
2008-05-01
First posted
2006-04-17
Last updated
2006-04-17

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00315081. Inclusion in this directory is not an endorsement.