Characterization of Macroprolactinemia

This study has been completed.
Sponsor:
Information provided by:
Kansai Medical University
ClinicalTrials.gov Identifier:
NCT00436111
First received: February 15, 2007
Last updated: NA
Last verified: February 2007
History: No changes posted
  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

Resource links provided by NLM:


Further study details as provided by Kansai Medical University:

Study Start Date: January 2005
Estimated Study Completion Date: December 2006
  Eligibility

Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Criteria

Inclusion Criteria:

  • Clinical diagnosis of hyperprolactinemia
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00436111

Locations
Japan
Kansai Medical University
Osaka, Japan, 570-8506
Sponsors and Collaborators
Kansai Medical University
Investigators
Study Chair: Naoki Hattori, M.D., Ph.D. Department of Pharmacology, Kansai Medical University