Non-interventional Study of Patients Using Norditropin® for Growth Hormone Deficiency or Turner Syndrome
NCT ID: NCT01604161
Last Updated: 2015-07-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
2016 participants
OBSERVATIONAL
2005-05-31
2015-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Somatropin
somatropin
Collection of safety and efficacy data in connection with use of somatropin (Norditropin®) in daily clinical practice.
Interventions
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somatropin
Collection of safety and efficacy data in connection with use of somatropin (Norditropin®) in daily clinical practice.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients with malignant tumors
* Women who are either pregnant or likely to be pregnant
* Known or suspected allergy to study product(s) or related products
ALL
No
Sponsors
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Novo Nordisk A/S
INDUSTRY
Responsible Party
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Principal Investigators
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Global Clinical Registry (GCR, 1452)
Role: STUDY_DIRECTOR
Novo Nordisk A/S
Locations
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Tokyo, , Japan
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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GH-3910
Identifier Type: -
Identifier Source: org_study_id
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