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Terminated No phase listed Observational Results available

A Study to Evaluate Growth in Participants Treated With Somatropin (Nutropin) Using NuSpin Device

ClinicalTrials.gov ID: NCT01243892

Public ClinicalTrials.gov record NCT01243892. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 9:22 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase IV, Open Label, Multicenter, Case-controlled Study of Growth in Patients Using the Nutropin AQ® Nuspin®

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase IV, open label, case-controlled, observational study to evaluate the age-adjusted cumulative height velocity in pre-pubertal isolated growth hormone deficient (IGHD) and idiopathic short stature (ISS) participants receiving daily doses of somatropin (recombinant human growth hormone \[rhGH\]; Nutropin) using NuSpin device compared to historical controls from the national cooperative growth study (NCGS).

Study identification

NCT ID
NCT01243892
Recruitment status
Terminated
Study type
Observational
Phase
Not listed
Lead sponsor
Genentech, Inc.
Industry
Enrollment
18 participants

Conditions and interventions

Interventions

Device · Drug

Eligibility (public fields only)

Age range
2 Years to 14 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2010
Primary completion
Jul 31, 2011
Completion
Jul 31, 2011
Last update posted
Nov 30, 2016

2010 – 2011

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Not listed Birmingham Alabama 35233
Not listed Scottsdale Arizona 85258
Not listed Sacramento California 95819
Not listed San Diego California 92123
Not listed Greenwood Village Colorado 80111
Not listed Palm Bay Florida 32905
Not listed Pembrook Pines Florida 33028
Not listed Atlanta Georgia 30342
Not listed Wheaton Illinois 60187
Not listed Minneapolis Minnesota 55455
Not listed Mount Kisco New York 10549
Not listed New Rochelle New York 10801
Not listed Columbus Ohio 43235
Not listed Knoxville Tennessee 37916

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01243892, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 30, 2016 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01243892 live on ClinicalTrials.gov.

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