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Clinical Trial Summary

Objectives: To evaluate the efficacy and safety of one year treatment based on daily doses of exogenous growth hormone (GH) in patients with traumatic spinal cord injury. The first six months the pharmacological treatment will be associated to rehabilitation treatment. The main hypothesis is that GH can improve motor function of patients with traumatic spinal cord injury below the lesion level. The hypothesis is based on possible effects of GH at muscle and synaptic level. GH can also promote axonal growth and regeneration. Design: Clinical trial placebo-controlled, double-blind intervention with blind evaluation by third parties and blinding in the analysis of data (triple-blind design). Duration of intervention and monitoring: 364 days. Primary outcome measures. Changes of the American Spinal Injury Association (ASIA) scale (motor score)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01329757
Study type Interventional
Source Hospital Nacional de Parapléjicos de Toledo
Contact
Status Completed
Phase Phase 3
Start date April 2011
Completion date November 2015

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