Trials / Completed
CompletedNCT00694863
Treatment With Synthetic ACTH in High Risk Patients With Membranous Nephropathy
Treatment With Synthetic Adrenocorticotropic Hormone (ACTH) in Patients With Membranous Nephropathy and High Risk for Renal Failure. A Pilot Study
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 20 (actual)
- Sponsor
- Radboud University Medical Center · Academic / Other
- Sex
- All
- Age
- 18 Years – 95 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine whether treatment with long-acting synthetic adrenocorticotropic hormone is in the treatment of patients with idiopathic membranous nephropathy and high for renal failure.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | tetracosactide hexacetaat | Intramuscular injections with tetracosactide hexacetaat (Synacthen Depot) 1ml a 1mg/ml. Treatment for 9 months with an increasing dosage from once per 2 weeks to twice a week. |
Timeline
- Start date
- 2008-07-01
- Primary completion
- 2010-12-01
- Completion
- 2012-12-01
- First posted
- 2008-06-11
- Last updated
- 2013-01-07
Locations
1 site across 1 country: Netherlands
Source: ClinicalTrials.gov record NCT00694863. Inclusion in this directory is not an endorsement.