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Safety and Efficacy of Long-term Somatropin Treatment in Adults (NordiWIN)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01543880
Recruitment Status : Completed
First Posted : March 5, 2012
Last Update Posted : April 29, 2015
Information provided by (Responsible Party):
Novo Nordisk A/S

Brief Summary:
This study is conducted in Europe. The aim of the study is to evaluate safety and efficacy in adults treated with somatropin (Norditropin®).

Condition or disease Intervention/treatment
Growth Hormone Disorder Adult Growth Hormone Deficiency Drug: somatropin

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Study Type : Observational
Actual Enrollment : 752 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Non-interventional Study of Safety and Efficacy of Long-term Somatropin Treatment in Adults
Study Start Date : July 2003
Actual Primary Completion Date : December 2013
Actual Study Completion Date : June 2014

Group/Cohort Intervention/treatment
Users of somatropin Drug: somatropin
Prescribed at the discretion of the treating physician according to product labelling

Primary Outcome Measures :
  1. Number of adverse events [ Time Frame: Up to 10 years ]

Secondary Outcome Measures :
  1. BMI (Body Mass Index) [ Time Frame: Up to 10 years ]
  2. HbA1c change [ Time Frame: Up to 10 years ]
  3. IGF-I (Insulin-Like Growth Factor I) [ Time Frame: Up to 10 years ]

Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Adults in need of somatropin or current users

Inclusion Criteria:

  • In need of somatropin or current user

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01543880

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Mainz, Germany, 55127
Sponsors and Collaborators
Novo Nordisk A/S
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Study Director: Global Clinical Registry (GCR, 1452) Novo Nordisk A/S

Additional Information:
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Responsible Party: Novo Nordisk A/S Identifier: NCT01543880     History of Changes
Other Study ID Numbers: GH-1931
First Posted: March 5, 2012    Key Record Dates
Last Update Posted: April 29, 2015
Last Verified: April 2015

Additional relevant MeSH terms:
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Dwarfism, Pituitary
Bone Diseases, Developmental
Bone Diseases
Musculoskeletal Diseases
Bone Diseases, Endocrine
Pituitary Diseases
Hypothalamic Diseases
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Endocrine System Diseases