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Safety and Efficacy of Wendan Decoction in Acute Moderated to Severe Brain Injury

Acute Brain Injury Clinical Trial

Official title:
A Randomized Controlled Trial of Wendan Decoction as a Palliative Treatment for Acute Brain Injury

Clinical Trial Summary

Efficacy and safety of Traditional Chinese Medicine (Wendan decoction) combined with conventional neurologic intensive care in patients with acute moderated to severe brain injury in early stage - A randomized controlled study.

Clinical Trial Description

This study adopted a prospective, randomized controlled design. All eligible patients included in the study agreed to participated and signed the informed consent from and the study procedures were approved by the ethical committee of Taichung Tzu Chi general hospital (REC103-26). Patients were recruited from the neurosurgery department of Taichung Tzu Chi general hospital between June 2014 and July 2015. A total of 60 patients were enrolled in this study and randomized into intervention group and control group. All patients of both groups were enrolled within 14 days after episode and a follow-up interview until 6 months from the onset. The intervention group mean regular neuro-intensive care combined TCM and the intervention group mean only neuro-intensive care. But there are 7 patients in intervention group and 12 patients in control group quit out this study ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03851809
Study type Interventional
Source Taichung Tzu Chi Hospital
Contact
Status Completed
Phase Phase 2/Phase 3
Start date June 1, 2014
Completion date January 31, 2016
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