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Trial · Interventional

CompletedPhase 4Results postedRegistry data

Long-Term Growth and Skeletal Effects of Early Growth Hormone Treatment in Turner Syndrome

NCTNCT00266656 (opens ClinicalTrials.gov in a new tab)Other id10088Other idB9R-US-GDGH

Overview

Status
Completed
Phase
Phase 4
Enrollment
69 participants (actual)
Sponsor
Eli Lilly and Company · Industry
Design
Not randomized · Open label (no masking)
Countries
1 country

United States

Start
Dec 2005
Primary completion
Sept 2015
Completion
Sept 2015
First posted
19 Dec 2005 (estimated)
Last update posted
31 Mar 2017
Conditions
Turner Syndrome

Timeline

1 trial · 1 completed · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
200620082010201220142016
  1. Ph 4

    Long-Term Growth and Skeletal Effects of Early Growth Hormone Treatment in Turner Syndrome

    NCT00266656

    Dec 2005 to Sept 2015

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

This is an extension study that will gather long-term data on the effect of early growth hormone (GH) treatment on adult height and other aspects of health and development in girls with Turner syndrome. The main purpose is to determine whether girls who received 2 years of GH treatment before 6 years of age achieve taller adult height than girls who were untreated during this time. The study will also look at middle ear and hearing function, and cognitive and behavioral development. Protocol completion is defined as attainment of height velocity less than or equal to 1.0 cm/year, or bone age greater than or equal to 15 years.

Interventions

  • HumatropeDrug

Arms2

  • Experimental

    Experimental 1 Control

    No drug administration in B9R-US-GDFG (NCT00406926). Humatrope according to investigator's clinical practice and guided by the approved package insert on whether treatment is given.

  • Experimental

    Experimental 2 Humatrope

    Humatrope according to investigator's clinical practice and guided by the approved package insert on whether treatment is given.

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Most Mature Height Standard Deviation Score (SDS)

    Time frame · Baseline through End of Study (10 years)

    Registry description

    SDS reports the number of standard deviations from the mean for age and sex for an individual measurement (normal range is -2 to +2 SDS). Height SDS is derived by subtracting the population mean from individual's height value and then dividing that difference by the population standard deviation. Greater height SDS values indicate greater height.

Secondary outcomes(8)
  1. Height SDS at Various Ages

    Time frame · Age 10, Age 13, Age 16

    Registry description

    SDS reports the number of standard deviations from the mean for age and sex for an individual measurement (normal range is -2 to +2 SDS). Height SDS is derived by subtracting the population mean from individual's height value and then dividing that difference by the population standard deviation. Greater height SDS values indicate greater height.

  2. Age at Attainment of Tanner 2 Breast Development

    Time frame · Baseline through End of Study (10 years)

    Registry description

    The Tanner 2 breast development is the age at first evidence of breast development.

  3. Chronological Age at First Visit Participant Attained Bone Age of 14.5 Years

    Time frame · Baseline through End of Study (10 years)

    Registry description

    Bone age was measured by standard radiograph, x-ray at baseline and annually for 10 years or until attainment of height velocity less than or equal to 1.0 centimeter per year (cm/year) and bone age greater or equal to 15 years.

  4. Reports of Serious Adverse Events

    Time frame · Baseline through End of Study (10 years)

    Registry description

    Number of serious adverse events (SAEs) reported. Any adverse event from this study that results in one of the following outcomes, or is significant for any other reason were reported as an SAE: death, initial or prolonged inpatient hospitalization, a life-threatening experience (that is, immediate risk of dying), persistent or significant disability/incapacity, congenital anomaly/birth defect in the offspring of a study subject, significant for any other reason (includes cancer, other than superficial, and basal cell or squamous cell carcinomas of the skin, that did not meet other serious adverse event criteria). A summary of other nonserious AEs, and all SAE's, regardless of causality, is located in the Reported Adverse Events section.

  5. Percentage of Participants With Occurrence of Pre-specified Clinically Relevant Events

    Time frame · Baseline through End of Study (10 years)

    Registry description

    Percentage of participants for whom certain non-serious, pre-specified adverse events (AEs; those that are commonly observed in Turner syndrome or are known to be related to GH treatment: impaired glucose tolerance, diabetes mellitus, hypothyroidism, benign intracranial hypertension, scoliosis, slipped capital femoral epiphysis, solid tumor/leukemia, pancreatitis, ear infections, and high blood pressure) are reported.

  6. Percentage of Participants With Abnormal Tympanometry Results

    Time frame · Baseline, Age 10, Age 16, End of Study (10 years)

    Registry description

    Percentage of participants with abnormal tympanometry \[defined as middle ear dysfunction / middle ear effusion / patent pressure equalizer tube or possible tympanic membrane perforation\] results at baseline, age 10 years, and age 16 years or endpoint.

  7. Percentage of Participants With Prevalence of Abnormal Audiometry Results

    Time frame · Baseline, Age 10, Age 16, End of Study (10 years)

    Registry description

    Percentage of participants with abnormal Audiometry results at baseline, age 10 years, and age 16 years or endpoint. Prevalence was calculated as number of participants with abnormal hearing divided by number of participants with measurable pure tone audiometry results at that visit.

  8. Percentage of Participants With Abnormal Audiometry Results Based on Pure Tone Average (PTA)

    Time frame · Baseline, Age 10, Age 16, End of Study (10 years)

    Registry description

    Percentage of participants with abnormal Audiometry results at baseline, age 10 years, and age 16 years or endpoint. PTA is defined as the average of pure tone hearing thresholds at 500, 1000 and 2000 Hz (Hertz), calculated separately for each ear and for each testing method (air or bone); normal PTA is defined as pure tone hearing threshold less than or equal to 20 dB HL (decibels Hearing Level), and abnormal PTA is defined as pure tone hearing threshold greater than 20 DB HL.

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

Primary outcome results

Primary outcomeMean· Baseline through End of Study (10 years)

Most Mature Height Standard Deviation Score (SDS)

GroupValue (standard deviation score)Spread
Early Treated-1.371.09
Early Untreated-1.601.21
Secondary and other outcome results(7)
Secondary outcomeMean· Age 10, Age 13, Age 16

Height SDS at Various Ages

GroupValue (Standard deviation score)Spread
Early Treated-0.661.16
Early Untreated-1.281.17
Secondary outcomeMean· Baseline through End of Study (10 years)

Age at Attainment of Tanner 2 Breast Development

GroupValue (years)Spread
Early Treated11.800.26
Early Untreated12.140.31
Secondary outcomeMean· Baseline through End of Study (10 years)

Chronological Age at First Visit Participant Attained Bone Age of 14.5 Years

GroupValue (years)Spread
Early Treated14.640.25
Early Untreated15.260.23
Secondary outcomeNumber· Baseline through End of Study (10 years)

Reports of Serious Adverse Events

GroupValue (events)
Early Treated8
Early Untreated5
Secondary outcomeNumber· Baseline through End of Study (10 years)

Percentage of Participants With Occurrence of Pre-specified Clinically Relevant Events

GroupValue (percentage of participants)
Early Treated13.9
Early Untreated18.2
Secondary outcomeNumber· Baseline, Age 10, Age 16, End of Study (10 years)

Percentage of Participants With Abnormal Tympanometry Results

GroupValue (percentage of participants)
Early Treated44.4
Early Untreated54.5
Secondary outcomeNumber· Baseline, Age 10, Age 16, End of Study (10 years)

Percentage of Participants With Prevalence of Abnormal Audiometry Results

GroupValue (percentage of participants)
Early Treated52.8
Early Untreated48.5

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther events
Early TreatedHumatrope administered according to investigator's clinical practice and guided by the approved package insert. Humatrope administered in B9R-US-GDFG (NCT00406926).–6 / 3634 / 36
Early UntreatedHumatrope administered according to investigator's clinical practice and guided by the approved package insert. Control: Humatrope was not administered in B9R-US-GDFG (NCT00406926).–5 / 3332 / 33

Each cell reads participants affected / participants at risk, as the registry posted them.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies0

Studies that cite this trial.

No study cites this trial.

Eligibility

Who could join, as posted.

Sex
Female
Age
from 4 Years up to 20 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Previously randomized in study B9R-US-GDFG (NCT00406926) * Karyotype-proven Turner syndrome Exclusion Criteria: * Immediate family members of study site personnel directly affiliated with the study

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