Characterization of Macroprolactinemia
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Purpose
The purpose of this study is to clarify the nature of macroprolactin which has recently been highlighted because of the high prevalence and a diagnostic pitfall of hyperprolactinemia. The results of this study are beneficial for the patients to whom unnecessary medications and unnecessary radiological examinations have been performed.
We used the remained serum samples taken for routine prolactin determination during the past several years. Since the blood was basically taken to examine the causes of hyperprolactinemia and only remained serum samples were used for this study, the Ethics Committee of Kobe City General Hospital judged that it was not required to obtain approval number.
| Condition |
|---|
|
Hyperprolactinemia |
| Study Type: | Observational |
| Study Design: | Observational Model: Defined Population Observational Model: Natural History Time Perspective: Longitudinal Time Perspective: Retrospective |
Eligibility| Genders Eligible for Study: | Both |
Inclusion Criteria:
- Clinical diagnosis of hyperprolactinemia
Contacts and Locations| Japan | |
| Kansai Medical University | |
| Osaka, Japan, 570-8506 | |
| Study Chair: | Naoki Hattori, M.D., Ph.D. | Department of Pharmacology, Kansai Medical University |
More Information
Publications:
| ClinicalTrials.gov Identifier: | NCT00436111 History of Changes |
| Other Study ID Numbers: | KK-2007-1 |
| Study First Received: | February 15, 2007 |
| Last Updated: | February 15, 2007 |
| Health Authority: | Japan: Ministry of Education, Culture, Sports, Science and Technology |
Keywords provided by Kansai Medical University:
|
hyperprolactinemia autoantibody |
Additional relevant MeSH terms:
|
Hyperprolactinemia Hyperpituitarism Pituitary Diseases Hypothalamic Diseases |
Brain Diseases Central Nervous System Diseases Nervous System Diseases Endocrine System Diseases |
ClinicalTrials.gov processed this record on May 21, 2013