Skip to content

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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03789344
Enrollment
240
Registered
2018-12-28
Start date
2018-12-01
Completion date
2020-12-30
Last updated
2018-12-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Percutaneous Coronary Intervention

Keywords

acupuncture, PCI

Brief summary

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

Interventions

OTHERacupuncture

Acupuncturists apply the seven-days' electro-acupuncture treatment on the acupoints of Neiguan points and Daling points for 30min per day.

OTHERPsychotherapy

Subjects in psychotherapy group would be accepted 20mins- psychotherapy per day.

Blank control subjects would be observed only during this investigation.

Sponsors

Huan Wang, MD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* The

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline Heart Rate Variability at 7 daysat 1day before and 7 days after percutaneous coronary interventionThe primary efficacy variable was the heart rate variability of patients accepted the PCI treatment between control group

Secondary

MeasureTime frameDescription
Scores of HAM-A1day before, 7,14 days after the intervenescores of HAM-A were recorded on 1day before, 7,14 days after the intervene
Scores of AIS1day before, 7,14 days after the intervenescores of AIS were recorded on 1day before, 7,14 days
Scores of HRSD1day before, 7,14 days after the intervenescores of HRSD were recorded on 1day before, 7,14 days

Other

MeasureTime frameDescription
inflammation mediators level in blood1day before, 7days after the intervenethe blood level of IL-6 and Hs-CRP were detected

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026