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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00881283
Other study ID # 2008-p-001379
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date September 8, 2008
Est. completion date March 30, 2010

Study information

Verified date August 2020
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine whether subjects who have been affected by Cushing's disease in the past maintain some different characteristics compared with subjects who have never been diagnosed with the disease.


Recruitment information / eligibility

Status Terminated
Enrollment 1
Est. completion date March 30, 2010
Est. primary completion date March 30, 2010
Accepts healthy volunteers No
Gender Female
Age group 35 Years to 55 Years
Eligibility Inclusion Criteria:

- patients who have been cured of Cushing's disease at least 5 years ago.

Exclusion Criteria:

- patients who have been cured of Cushing's disease more than 15 years ago.

Study Design


Locations

Country Name City State
United States Neuroendocrine Clinical Center Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary adipokine measurements baseline
See also
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Completed NCT00889525 - Study of Cabergoline in Treatment of Corticotroph Pituitary Tumor Phase 3
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Completed NCT01794793 - Study to Allow Access to Pasireotide for Patients Benefiting From Pasireotide Treatment in Novartis-sponsored Studies Phase 4
Completed NCT00434148 - Safety and Efficacy of Different Dose Levels of Pasireotide in Patients With de Novo, Persistent or Recurrent Cushing's Disease Phase 3
Completed NCT03346954 - Impact of [11C]-Methionine PET/MRI in the Detection of Pituitary Adenomas Secreting ACTH and Causing Cushing's Disease N/A
Withdrawn NCT01925092 - Mifepristone in Children With Refractory Cushing's Disease Phase 3
Completed NCT01582061 - An Open-label, Multi-center, Expanded Access Study of Pasireotide s.c. in Patients With Cushing's Disease. Phase 3
Recruiting NCT03708900 - Pharmacokinetic (PK), Pharmacodynamic (PD) and Tolerability of Osilodrostat in Pediatric Patients With Cushing's Disease Phase 2
Terminated NCT00612066 - Rosiglitazone in Treating Patients With Newly Diagnosed ACTH-Secreting Pituitary Tumor (Cushing Disease) Phase 2