Randomized Controlled Trials of Electro-acupuncture Effects on Perioperative Anxiety in Patients Treated With PCI

Not Applicable

• Conditions: Percutaneous Coronary Intervention
• Interventions: Other: blank control; Other: acupuncture; Other: Psychotherapy

• Registration Number: NCT03789344
• Lead Sponsor: Huan Wang, MD

Brief Summary

Randomized Controlled Trials of Electro-acupuncture Effects on Perioperative Anxiety in Patients Treated with PCI

Detailed Description

Not available

Study Timeline

• Status Verified: 2018-12
• Study Start: 2018-12-01
• Study First Submitted: 2018-12-24
• Study First Submitted QC: 2018-12-26
• Last Update Submitted: 2018-12-26
• Study First Posted: 2018-12-28
• Last Update Posted: 2018-12-28
• Primary Completion: 2019-05-01
• Study Completion: 2020-12-30

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 240

Inclusion Criteria

• The main inclusion criteria were patients who underwent coronary angiography. Patients suffer from Generalized anxiety disorder(GOD).

Exclusion Criteria

• The exclusion criteria were as follows: patients with chronic renal failure, chronic liver disease, bone disorders, and/or thyroid disorders.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
blank control	blank control	-
Acupuncture treatment	acupuncture	-
Psychotherapy	Psychotherapy	-

Primary Outcome Measures

Name	Time	Method
Change from Baseline Heart Rate Variability at 7 days	at 1day before and 7 days after percutaneous coronary intervention	The primary efficacy variable was the heart rate variability of patients accepted the PCI treatment between control group

Secondary Outcome Measures

Name	Time	Method
Scores of HAM-A	1day before, 7，14 days after the intervene	scores of HAM-A were recorded on 1day before, 7，14 days after the intervene
Scores of HRSD	1day before, 7，14 days after the intervene	scores of HRSD were recorded on 1day before, 7，14 days
Scores of AIS	1day before, 7，14 days after the intervene	scores of AIS were recorded on 1day before, 7，14 days

Trial Locations

Locations (1)

PLA General Hospital; 🇨🇳 Beijing, Beijing, China