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Efficacy Study of Low-Dose Hydrocortisone Treatment for Fibromyalgia
This study has been completed.

First Received on October 10, 2005.   Last Updated on June 18, 2007   History of Changes
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

Resource links provided by NLM:


Further study details as provided by Ludwig-Maximilians - University of Munich:

Primary Outcome Measures:
  • Fibromyalgia symptoms [ Time Frame: 3 months ]
  • Pain scores [ Time Frame: 3 months ]
  • Tenderness at tender points [ Time Frame: 3 months ]

Secondary Outcome Measures:
  • Chronic stress symptoms [ Time Frame: 3 months ]
  • Health-related quality of life [ Time Frame: 3 months ]
  • Life satisfaction [ Time Frame: 3 months ]

Enrollment: 30
Study Start Date: May 2003
Study Completion Date: June 2007
Detailed Description:

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:

  • Impaired glucocorticoid signaling is associated in a failure to terminate the chronic stress response seen in patients with FMS.
  • Low-dose hydrocortisone in patients with FMS results in a reduction in pain and other stress-related symptoms of FMS

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:

  • Improvements in FMS symptoms representing (functional) hypocortisolism
  • Increased pain threshold

Expected results:

  • Moderate reductions in physical impairment, fatigue, and stiffness
  • Improvements in sleep quality
  • Decline in pain intensity Inclusion criteria
  • FMS diagnosis according to the American College of Rheumatology 1990 Criteria
  • Age between 18 and 60 years

Exclusion criteria

  • Disease states representing contraindications to the administration of glucocorticoids (tuberculosis, gastric- and duodenal ulcers, Cushing’s disease, osteoporosis, hypertension, pregnancy and lactation, psychosis, glaucoma, diabetes mellitus, thrombophilia, active or chronic bacterial or viral infections, hypothyreosis, cirrhosis).
  • Severe or chronic somatic diseases.
  • Psychiatric diseases according to DSM-IV (except PTSD, minor depressive episodes, minor personality disorders).
  • Body weight >20% above or below normal.
  • Changes in pharmacologic or psychotherapeutic management less than 3 months ago.
  • Age < 18 years

Proposed outcome measures

  • Primary: FMS symptoms, pain scores, tenderness at tender points
  • Secondary: Chronic stress symptoms, health-related quality of life

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
Criteria

Inclusion Criteria:

  • FMS diagnosis according to the American College of Rheumatology 1990 Criteria.
  • Age between 18 and 60 years

Exclusion Criteria:

  • Disease states representing contraindications to the administration of glucocorticoids (tuberculosis, gastric- and duodenal ulcers, Cushing’s disease, osteoporosis, hypertension, pregnancy and lactation, psychosis, glaucoma, diabetes mellitus, thrombophilia, active or chronic bacterial or viral infections, hypothyreosis, cirrhosis)
  • Severe or chronic somatic diseases
  • Psychiatric diseases according to DSM-IV (except PTSD, minor depressive episodes, minor personality disorders)
  • Body weight >20% above or below normal
  • Changes in pharmacologic or psychotherapeutic management less than 3 months ago
  • Age < 18 years
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00236925

Locations
Germany
Ludwig-Maximilians University
Muenchen, Bavaria, Germany, 81377
Sponsors and Collaborators
Ludwig-Maximilians - University of Munich
University of Zurich
Investigators
Principal Investigator: Gustav Schelling, MD, PhD Ludwig-Maximilians - University of Munich
  More Information

Additional Information:
Publications:
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

Keywords provided by Ludwig-Maximilians - University of Munich:
Fibromyalgia
Cortisol
Hydrocortisone
Stress

Additional relevant MeSH terms:
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

ClinicalTrials.gov processed this record on February 09, 2012