CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 11 enrolled
Drug / intervention
Human Growth Hormone (1-134) +1 moredrug
Likely dose
Human Growth Hormone (1-134) 0.2 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01007071
NCT01007071Phase 3Completed

Effects of Growth Hormone on Cognition and Cerebral Metabolism in Adults

Stanford University·interventional·Posted Nov 3, 2009·Updated Nov 17, 2017

In Brief

A Phase 3 clinical trial evaluating Human Growth Hormone (1-134) and Placebo for Hypopituitarism. Completed, enrolled 11 participants across 1 site.

Detailed Summary

Patients with Growth hormone (GH) deficiency often report impaired quality of life and difficulty with mental functioning. It has been suggested that GH replacement in such patients leads to improvement in cognitive function. The aim of this study is to elucidate the effects of GH replacement in patients with GH deficiency on cognitive function using structural and functional neuroimaging and cognitive testing.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHypopituitarism
CountriesUnited States
CollaboratorsGenentech, Inc.

Timeline

Phase 3CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedNov 3, 2009
Enrollment StartNov 1, 2009
Primary CompletionDec 12, 2012
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 16.7 years ago

Interventions

Human Growth Hormone (1-134)drug

Subjects randomized to human growth hormone (1-134) for 16 weeks. In this arm, growth hormone is dosed sc on a daily basis and increased over first 6 weeks (Men: start at 0.2 mg sc/d, increase to 0.6 mg sc/d after 4 weeks. Women, postmenopausal: start at 0.3 mg sc/d, increase to 0.9 mg sc/d after 4 weeks. Women premenopausal or on estrogen: start at 0.6 mg sc/d, increase to 1.3 mg sc/d after 4 weeks.) Dose adjustments based on serum IGF-1 levels at 6 and 12 weeks, with final IGF-1 measurement for efficacy performed at 16 weeks, with goal in range of -0.5 SD to +2SD. An elevated serum IGF-1 value will result in a 20% dose reduction in GH in an active and random placebo patient. Similarly, a low serum IGF-1 will result in a 20% dose increase in an active and random placebo subject.

Placebodrug

Subjects randomized to placebo