EPC quantification after G-CSF stimulation in healthy volunteers
Completed
- Conditions
- cancermalignancy10027655
- Registration Number
- NL-OMON31566
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
1.The volunteer must be >= 18 years of age
2.The volunteer must be healthy
meaning having no relevant medical history and havind no clinical signs of intercurrent infection at physical exam at start of the study
3.The volunteer mustn*t have known hypersensitivity to the to be administrated drugs (filgrastim®)
4.The patient must have given written informed consent
5. women wild child bearing potential must have a negative serum pregnancy test 48 hrs before start
Exclusion Criteria
Any other condition by which the patient doesn*t meet the inclusion criteria
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Primary objective is:<br /><br>To determine whether a single subcutaneous injection of G-CSF induces an<br /><br>immediate (within six hours) release of bone marrow progenitor cells in healthy<br /><br>volunteers.</p><br>
- Secondary Outcome Measures
Name Time Method <p>nvt</p><br>