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| Sponsor: | Ludwig-Maximilians - University of Munich |
|---|---|
| Collaborator: |
University of Zurich |
| Information provided by: | Ludwig-Maximilians - University of Munich |
| ClinicalTrials.gov Identifier: | NCT00236925 |
Purpose
This study is based on clinical findings that some patients with fibromyalgia have a tendency towards lower levels of the stress hormone cortisol. The hypothesis to be tested in this study is that the administration of a very low-dose of cortisol which has no side effects corrects this deficiency and results in an improvement of symptoms
| Condition | Intervention |
|---|---|
|
Fibromyalgia |
Drug: Hydrocortisone (low-dose) |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Crossover Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | A Double-Blind Crossover Within Subject Study on Low-Dose Hydrocortisone for Fibromyalgia |
| Enrollment: | 30 |
| Study Start Date: | May 2003 |
| Study Completion Date: | June 2007 |
Fibromyalgia (FMS) is regarded as one of the most important chronic pain syndromes with a high prevalence in the general population.
Hypotheses to be tested in this study:
Intervention:
2 x 5 mg of hydrocortisone given at noon and in the evening
Study design:
Double-blind, randomized, cross-over, within-subject
Presumed mechanism of main hydrocortisone effect:
Expected results:
Exclusion criteria
Proposed outcome measures
Possible benefit and use of data from the trial
This trial could help to identify glucocorticoid resistance as a major mechanism underlying the sustained stress – reactions seen in FMS and establish low-dose hydrocortisone as a useful drug for treatment of stress-related disorders.
Eligibility| Ages Eligible for Study: | 18 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Germany | |
| Ludwig-Maximilians University | |
| Muenchen, Bavaria, Germany, 81377 | |
| Principal Investigator: | Gustav Schelling, MD, PhD | Ludwig-Maximilians - University of Munich |
More Information
| ClinicalTrials.gov Identifier: | NCT00236925 History of Changes |
| Other Study ID Numbers: | 348/02 |
| Study First Received: | October 10, 2005 |
| Last Updated: | June 18, 2007 |
| Health Authority: | Germany: Federal Institute for Drugs and Medical Devices |
|
Fibromyalgia Cortisol Hydrocortisone Stress |
|
Fibromyalgia Myofascial Pain Syndromes Muscular Diseases Musculoskeletal Diseases Rheumatic Diseases Neuromuscular Diseases Nervous System Diseases |
Cortisol succinate Hydrocortisone acetate Hydrocortisone Anti-Inflammatory Agents Therapeutic Uses Pharmacologic Actions |