Clinical Trials Directory

Trials / Completed

CompletedNCT01201863

Neuroendocrine Dysfunction in Traumatic Brain Injury: Effects of Testosterone Therapy

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
46 (actual)
Sponsor
Craig Hospital · Academic / Other
Sex
Male
Age
16 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to address 3 short term objectives; (1) Determine the effects of physiologic testosterone (T) therapy on neurological function and functional independence following traumatic brain injury (TBI) in hypogonadal men during inpatient rehabilitation; (2) Document the natural history of neuroendocrine dysfunction and recovery in men during inpatient rehabilitation after TBI; (3) Obtain data to validate the NIH toolbox, a novel assessment of neurological function for use in the TBI population; and 2 long-term objectives: (1) Utilize study findings to design a multicenter trial to further assess the impact of T therapy in hypogonadal men following TBI and (2) Impact TBI practice management with new information about neuroendocrine dysfunction after TBI and hormone treatments to improve outcomes.

Detailed description

This randomized, double blind, placebo-controlled pilot study assessed the hormonal status of men on admission to an inpatient TBI rehabilitation program. 498 consecutively admitted men for TBI rehabilitation were screened for participation in the study. 22 participants with low T who met all criteria were randomized into placebo (n=10), or physiologic T therapy (n=12). Of those with normal T who met all criteria, 24 were randomized into a follow up group. All participants were evaluated every two weeks for up to 12 weeks: hormone levels, FIM ratings and NIH Toolbox testing as able. There was participant drop out over time as participants were discharged from the hospital. The final analysis examined differences between the normal T, low T Treatment and low T placebo groups on hormone levels, FIM ratings and NIH Toolbox results at baseline and weeks 2, 4 and 6.

Conditions

Interventions

TypeNameDescription
DRUGAndrogel (Testosterone Gel)2.5 gram stickpacks administered with starting dosage of 5g increasing to a max of 10g.
OTHERPlacebo gel2.5 gram stickpacks with starting dose of 5g increasing to max of 10g.

Timeline

Start date
2010-09-01
Primary completion
2014-07-01
Completion
2014-07-01
First posted
2010-09-15
Last updated
2021-07-27
Results posted
2021-07-27

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01201863. Inclusion in this directory is not an endorsement.