Clinical Trials Directory

Trials / Unknown

UnknownNCT05413460

Acupoint Stimulation and Cranial Endovascular Treatment

Effect of Transcutaneous Electrical Acupoint Stimulation on Postoperative Complications After Cranial Endovascular Treatment

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
158 (estimated)
Sponsor
Zhihong LU · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

In this prospective randomized controlled trial, the subjects will be assigned to group transcutaneous electrical acupoint stimulation (TEAS) and group control (no intervention). The postoperative outcomes including NIHSS (National Institute of Health stroke scale) score, morbidity and mortality will be evaluated during hospital stay and by one year after surgery.

Conditions

Interventions

TypeNameDescription
DEVICEtranscutaneous electrical acupoint stimulationElectrodes are placed at acupoints and connected to the stimulator. Electrical stimulation is given during surgery.

Timeline

Start date
2022-07-26
Primary completion
2023-06-30
Completion
2023-06-30
First posted
2022-06-10
Last updated
2022-12-06

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05413460. Inclusion in this directory is not an endorsement.

Acupoint Stimulation and Cranial Endovascular Treatment (NCT05413460) · Clinical Trials Directory