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Search / Trial NCT00851942

Determination of Method-specific Normal Cortisol and Adrenal Hormone Responses to the Short Synacthen Test

Launched by CARDIFF UNIVERSITY · Feb 25, 2009

Trial Information

Current as of May 01, 2025

Completed

Keywords

Volunteer Hypoadrenalism Hypopituitarism Healthy Volunteers

ClinConnect Summary

Synacthen® is a synthetic analogue of ACTH which has been used since the 1960s to assess adrenal sufficiency. It is now well established as a first line test to investigate diseases of the hypothalamo-pituitary-adrenal axis and to assess adrenal function in patients on long-term corticosteroid therapy. Briefly, cortisol is measured before and after injection of 250 micrograms of Synacthen®. In a normal individual serum cortisol will rise to concentrations greater than an arbitrary value (typically 550 nmol/l) 30 minutes after administration of Synacthen®.

In 2004 the All Wales Clinical Bio...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Volunteers will be in self-proclaimed good health
  • Volunteers will be free of illness on the day of testing
  • Volunteers will not be taking drug therapy.
  • Patients will be free of intercurrent illness on the day of testing
  • Patients will have a confirmed diagnosis of hypoadrenalism or hypopituitarism
  • Exclusion Criteria:
  • Is pregnant or lactating. Females of childbearing potential must have a negative pregnancy test before enrollment onto the study. Non-child bearing potential is defined as post-menopausal for at least 1 year, surgical sterilisation or hysterectomy at least three months before the start of the study,
  • Is using corticosteroids,
  • has any significant intercurrent disease,
  • has a history of thyroid or other autoimmune disease,
  • has a previous history of hypersensitivity to Synacthen®,
  • has a previous history of asthma
  • has a history of allergic disorder
  • has any mental condition rendering the patient unable to understand the nature or possible consequences of the study, and/or evidence of an uncooperative attitude.

About Cardiff University

Cardiff University is a prestigious research institution located in Wales, known for its commitment to advancing knowledge and improving health outcomes through innovative clinical research. With a robust framework for conducting clinical trials, the university leverages its multidisciplinary expertise and state-of-the-art facilities to explore new therapeutic approaches and enhance patient care. Collaborating with healthcare partners and academic institutions, Cardiff University aims to translate research findings into practical applications, fostering a culture of scientific inquiry and excellence in clinical practices.

Locations

Cardiff, South Glamorgan, United Kingdom

Patients applied

0 patients applied

Trial Officials

Aled Rees, MB BCh, PhD

Principal Investigator

Cardiff University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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