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Clinical Trial Summary

The aim of this study is to evaluate the effect of acupuncture on inflammation and immune function after craniotomy. This study will be a single-center, parallel group clinical trial that will be conducted at Kyung Hee University Hospital at Gangdong, Seoul, Korea.


Clinical Trial Description

For Study group, The intervention will start no more than 48 hours after craniotomy and will be given once a day for 6 days (a total of 6 sessions within 8 days). Acupuncture, electroacupuncture, and intradermal acupuncture will be performed at every session.

For Control group, The subjects in the control group will only receive conventional treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02761096
Study type Interventional
Source Kyunghee University Medical Center
Contact
Status Completed
Phase N/A
Start date April 2016
Completion date November 2017

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