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N/A N=7 Health Services Research

Adrenal Suppression and Adrenal Recovery Induced by Megestrol Acetate

Adrenal Insufficiency

Enrolled (actual)
7
Serious AEs
0.0%
Results posted
Aug 2011
Primary outcome: Primary: Number of Participants With Adrenal Insufficiency — 7 participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
megestrol acetate (Drug)
Age
Older Adult · 65+ yrs
Sex
All
Sponsor
University of Arkansas
Primary completion
Dec 2004

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Adrenal Insufficiency
7
PRIMARY
Time Required for Recovery From Adrenal Suppression to Normal Adrenal Function
6; 2; 2; 2; 2; 2

Summary

Megestrol Acetate (MA) is a progesterone-like hormone that has been utilized as a birth control agent, chemotherapeutic drug, and more recently, to induce appetite and weight gain in patients malnourished as a result of radiation therapy, chemotherapy, cystic fibrosis, AIDS, or dementia. The mechanism of MA-stimulated appetite and weight gain is unknown. Although only approved to combat weight loss associated with AIDS and cancer, MA is frequently prescribed for long periods of time to prevent or reverse weight loss in nursing home residents and in elderly patients with serious illnesses in the community. Little data is available to support this practice. Among its many properties, MA acts as a partial glucocorticoid agonist, and long term and short term use of MA may results in adrenal suppression. The rapidity of the onset of MA-induced adrenal suppression and the time course of resumption of normal adrenal function after discontinuation of MA is completely unknown. As a consequence, it is unclear whether MA can be given safely for short periods of time or whether glucocorticoid administration is necessary after abruptly stopping MA treatment. The increased use of MA in the frail elderly, where even partial adrenal insufficiency may pose a substantial risk of adrenal crisis after an illness, requires a clear understanding of these issues. To address these concerns, we will evaluate adrenal function before, during, and after MA administration in healthy volunteers between the ages of 60 and 85 years.

Eligibility Criteria

Inclusion Criteria

  • Elderly males and females
  • Age 65-80 years
  • With stable (no history of urgent/ emergent care visits with health care provider/s in the preceding 2 months), medical conditions

Exclusion Criteria

Subjects will be excluded if they have a history of (H/O):

  • Dementia
  • Adrenal disease
  • Thromboembolism
  • Diabetes mellitus
  • Liver disease
  • Electrolyte abnormalities; or
  • Vaginal bleeding
  • Hypertriglyceridemia
  • CAD with CHF
  • Unstable depression
  • Schizophrenia; and
  • Morbidly obese subjects.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00575029). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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