No registrations found.
ID
Source
Brief title
Health condition
Hypercortisolism due to Cushing's disease
Sponsors and support
Dpt. of Internal Medicine, Endocrine Section
Rotterdam
The Netherlands
Intervention
Outcome measures
Primary outcome
- Achievement of normocortisolism
Secondary outcome
- Improvement of clinical symptoms of Cushing's disease
- Quality of life
- Glucose tolerance
- Pituitary adenoma size
- Bone metabolism (bone mineral density, bone formative and resorptive markers)
- Hemostasis
Background summary
In this trial patients with Cushing's disease will be treated medically using a stepwise approach with respectively SOM230, cabergoline and ketoconazole.
Study objective
Currently, no effective, non-toxic medical therapy is available for Cushing's disease. Corticotroph adenomas express both somatostatin receptor subtype 5 and dopamine receptors. SOM230 is a new somatostatin analog which binds to 4 of 5 somatostatin receptor subtypes. In vitro studies show that somatostatin analogs and dopamine agonists may potentiate each others effects. Dopamine agonists are also effective in a subset of patients with Cushing's disease. Finally, ketoconazole has apart from its adrenolytic effects, inhibitory effects on ACTH secretion by and cell growth of corticotroph tumor cells which are potentiated by SOM230. By combining these partially independent medical therapies which act through differential mechanisms, we aim at maximizing the number of patients with Cushing’s disease in whom normalization of cortisol production can be achieved.
Study design
Total study duration is 80 days, evaluation of patients will be performed at day 10, day 26, day 54 and day 80.
Intervention
Patients with Cushing's disease will be treated medically by the following stepwise approach:
- Patients will start with SOM230 (sc.), if this is not effective cabergoline (p.o.) will be added in an increasing dosage, finally when hypercortisolism persists, ketoconazole (p.o.) is added.
Total study duration is 80 days.
Department of Internal Medicine
Endocrine Section
R.A. Feelders
's Gravendijkwal 230
Rotterdam 3015 EC
The Netherlands
+31 (0)10 7040704
r.feelders@erasmusmc.nl
Department of Internal Medicine
Endocrine Section
R.A. Feelders
's Gravendijkwal 230
Rotterdam 3015 EC
The Netherlands
+31 (0)10 7040704
r.feelders@erasmusmc.nl
Inclusion criteria
1. Both naïve patients with Cushing’s disease and patients with residual hypercortisolism after recent transsphenoidal adenomectomy are eligible for enrolment.
2. Finally, patients with recurrent Cushing’s disease can also be included.
Exclusion criteria
1. Patients with poorly controlled diabetes mellitus indicated by a HbA1c % > 8.5 %.
2. Patients with a disturbed liver function indicated by serum bilirubin, ALAT, ASAT or alkaline phosphatase levels > 2.5 x ULN.
3. Patients with renal insufficiency indicated by serum creatinine levels > 2.0 x ULN
4. Patients who are already treated with cortisol lowering therapy can only be included after a wash-out period of 4 weeks followed by re-assessment for hypercortisolism
5. Patients with symptomatic cholelithiasis.
6. Patients with a history of pituitary irradiation.
7. Pregnant patients or patients who desire to become pregnant during the study period.
Design
Recruitment
Followed up by the following (possibly more current) registration
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL1322 |
NTR-old | NTR1379 |
CCMO | NL13656.078.07 |
ISRCTN | ISRCTN wordt niet meer aangevraagd |
OMON | NL-OMON30660 |