To Assess the Level of Adherence of Subjects Receiving SAIZEN® Via Easypod™ in Columbia
ECOS COL
Easypod Connect: A National, Multicentre, Observational Registry to Evaluate Adherence and Long Term Outcomes of Therapy in Paediatric Subjects Using "Easypod™" Electromechanical Device for Growth Hormone Treatment in Columbia
1 other identifier
observational
44
1 country
1
Brief Summary
This is a Columbian, Multicentre, Observational Study to evaluate Adherence and Long Term Outcomes of Therapy in paediatric subjects using easypod™ electromechanical device for growth hormone treatment and to assess the level of adherence of subject receiving SAIZEN® via easypod™.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jul 2014
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 22, 2013
CompletedStudy Start
First participant enrolled
July 31, 2014
CompletedFirst Posted
Study publicly available on registry
August 4, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2015
CompletedDecember 26, 2017
December 1, 2017
1.4 years
July 22, 2013
December 22, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Mean percent of daily recorded adherence
At least 6 months and up to 5 years
Secondary Outcomes (3)
Correlation of adherence and growth outcome after each year of SAIZEN® treatment with easypod™
At least 6 months and up to 5 years
Subject adherence profile based on age, gender, indication, self-injection or not, time on treatment
At least 6 months and up to 5 years
Correlation of adherence with current IGF-1 status (i.e. above, below or within normal ranges)
At least 6 months and up to 5 years
Interventions
Saizen (Somatropin) as per Summary of Product Characteristics administered by easypod™
Eligibility Criteria
Paediatric subjects (aged 2-18) who are taking SAIZEN® for registered indications using the easypod™ electromechanical device.
You may qualify if:
- Administered growth hormone via the easypod™ electromechanical device according to Summary of Product Characteristic (SmPC)
- Over the age of \>2 years
- Under \<18 years of age, or over 18 without fusion of growth plates
- Parent's or guardian's written informed consent, given before entering data into the observational study, with the understanding that the subject or parent/guardian may withdraw consent at any time without prejudice to future medical care. If the child is old enough to read and write, a separate assent form will be given as defined in the appropriate jurisdiction of each country
You may not qualify if:
- Subjects taking growth hormone in whom growth plates have fused (i.e. for taking growth hormone for it's metabolic effects)
- Contra-indications to SAIZEN® as defined in the SmPC
- Use of an investigational drug or participation in another interventional clinical study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Merck KGaA, Darmstadt, Germanylead
- Merck S.A. Columbiacollaborator
Study Sites (1)
For Recruiting Locations in Colombia
Please Contact the Merck KGaA Communication Center, Colombia
Related Publications (2)
Koledova, E. et al. (2017) Analysis of results from the global, 5-year Easypod™ Connect Observational Study (ECOS) study in children with growth disorders. 10th International Meeting for Pediatric Endocrinology; 2017 Sep 14-17; Washington, DC.
RESULTWit, JM. et al. (2017) Effect of adherence on the 2-year growth response to growth hormone treatment in prepubertal children with idiopathic isolated growth hormone deficiency participating in the EasypodTM Connect Observational Study (ECOS). 10th International Meeting of Paediatric Endocrinology; 2017 Sep 14-17; Washington, DC.
RESULT
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Medical Director
Merck S.A., Colombia, an affiliate of Merck KGaA, Darmstadt, Germany
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- OTHER
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 22, 2013
First Posted
August 4, 2014
Study Start
July 31, 2014
Primary Completion
December 31, 2015
Study Completion
December 31, 2015
Last Updated
December 26, 2017
Record last verified: 2017-12