Growth Hormone or Sildenafil as Therapies for Fatigue in Mild- Traumatic-brain-injury (MTBI)
Completed · Phase 1 · Has a placebo group
Conditions studied: Traumatic Brain Injury
In brief
The overall goal is to determine whether perceptual or performance fatigue can be reduced in MTBI patients with and without growth hormone (GH) deficiency by treating them in a crossover fashion based upon GH status. A battery of functional, fatigue, cognitive, imaging and blood flow tests will be performed to assess the efficacy of the two drug interventions, Growth hormone and Sildenafil.
Key facts
- Study ID
- NCT02114775
- Run by
- The University of Texas Medical Branch, Galveston
- People needed
- 34
- Starts
- 2014-12-12
- Expected to finish
- 2017-11-10
- Last updated by the study team
- 2018-02-05
Who can join
Age: 18 and older, up to 60. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or female with a diagnosis of mild TBI and 6 month post-injury. Age 18 to 60 years. Complaint of fatigue, with score of 3 or greater on questions 1, 2, or 3 of the Brief Fatigue Inventory.
You may not qualify if…
- Exclusion criteria (general)
- Significant heart, liver, kidney, blood or respiratory disease.
- Active coronary disease.
- Pregnancy.
- Alcohol or drug abuse.
- Unable to walk unassisted.
- Diabetes mellitus and anterior pituitary abnormalities diagnosed upon screening.
- Premorbid history of psychiatric disorder.
- Premorbid history of head trauma.
- Exclusion criteria (sildenafil/placebo group)
- Use of nitrates.
- Use of alpha blockers.
- Systolic blood pressure <100 or >150, diastolic blood pressure <60 or >90. This range is smaller than the acceptable range stated in the prescribing information for sildenafil (>90/50 and <170/110).
- Peripheral vascular disease.
- Use of a phosphodiesterase 5 inhibitor.
- Exclusion criteria (growth hormone/placebo group)
- Coumadin because of the risk of bleeding with daily injections of Recombinant Human Growth Hormone (rhGH) in the growth hormone (GH) arm of the study.
- Subjects who are deficient in cortisol or thyroid at screening will be excluded until hormone abnormalities have been corrected.
- Subjects with chronic pain who are being managed with narcotics will be excluded as the effects of central nervous system depressants may interfere with study test results.
Where it is running
- University of Texas Medical Branch — Galveston, Texas, United States
Full record on ClinicalTrials.gov
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