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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04272476
Other study ID # ChengduUTCM
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date January 2014
Est. completion date December 2019

Study information

Verified date February 2020
Source Chengdu University of Traditional Chinese Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates the activation on prefrontal cortex with acupuncture and moxibustion for major depressive disorder.Half of participants will receive the treatment of acupuncture and moxibustion, while the other participants will receive the fluoxetine.


Description:

Major depressive disorder (MDD) is a psychiatric condition with high morbidity, disability, suicide and recurrence rate and become the hot and difficult topics in the medical study. Given the unsatisfactory response rates of many FDA-approved antidepressants, acupuncture is increasingly considered an important alternative therapy. A large number of clinical trials have confirmed that acupuncture is a generally safe, effective, and well-tolerated therapy for depression, but for MDD, the acupuncture clinical trials were only reported out of China. According to the clinical symptoms in patients with MDD, the chief TCM patterns are liver qi constraint and heart yang insufficiency, and the secondary TCM patterns are blood stasis, qi and blood deficiency. So we propose to combine acupuncture with moxibustion and select Baihui (DU20), shenting(DU24), Neiguan (PC6), Hegu (LI4), Taichong (LV3), Zusanli(ST36), Zhongwan (RN 12) and Gaunyuan (RN4) to Soothe the Liver, regulating the heart, warm the yang qi, boost qi and invigorate blood for MDD. We hypothesize that the acupuncture's antidepressant effect is based on the neural network reconstructing mechanism through studying the cerebral cortex function, hippocampal synaptic plasticity, Neurons electrophysiological change. We will employ multi-disciplinary methods in neuropsychology, neuroimaging, computer science, and electrophysiology to explore the important mechanism underlying acupuncture and moxibustion treating MDD.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 2019
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- diagnostic criteria of CCMD-3 and DSM-4 depression;

- the score of PHQ-9 should be equal to or more than 15 points; the score of Hamilton Depression Rating Scale should be more than 18 points;

- without any drug treatment over the past 3 months

Study Design


Intervention

Other:
acupuncture and moxibustion

Drug:
Fluoxetine


Locations

Country Name City State
China Teaching Hospital of Chengdu University of Traditional Chinese Medicine Chengdu Sichuan

Sponsors (2)

Lead Sponsor Collaborator
Chengdu University of Traditional Chinese Medicine Massachusetts General Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Other The pHQ-9 score Screening criteria
Primary The Hamilton score as a measure of depressive degree Evaluating the patient's depressive degree 1, 2, 4, 6, 8 weeks after treatment
Primary The fNIRS score as a measure of prefrontal oxyhemoglobin Evaluating the patient's prefrontal oxyhemoglobin 1, 2, 4, 6, 8 weeks after treatment
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