Clinical Trials Directory

Trials / Completed

CompletedNCT05724095

Electrical Acupoint Stimulation Reduces Intrathecal Anesthesia Induced Hypotension

Electrical Acupoint Stimulation Alleviates Hypotension After Spinal Anesthesia in Parturients: a Prospective Randomized Controlled Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
90 (actual)
Sponsor
Zhihong LU · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The parturients may suffer from hypotension after spinal anesthesia and the incidence could be as high as 70-80% when pharmacological prophylaxis is not used. Acupuncture was reported to treat hypotension both in human and animal studies. Possible mechanisms include modulating cardiovascular and sympathetic system. In this prospective, double-blinded, randomized clinical trial, we tend to investigate the effect of transcutaneous electric acupoint stimulation (TEAS) on hypotension in parturients undergoing cesarean section.

Conditions

Interventions

TypeNameDescription
OTHERhigh frequency acupoint stimulationelectrodes are attached to area of acupoints and electrical stimulation at 10/50 Hz is given
OTHERlow frequency acupoint stimulationelectrodes are attached to area of acupoints and electrical stimulation at 2/10 Hz is given
OTHERelectrodes attachedelectrodes are attached to area of acupoints

Timeline

Start date
2023-02-20
Primary completion
2023-08-29
Completion
2023-08-29
First posted
2023-02-13
Last updated
2023-12-19

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05724095. Inclusion in this directory is not an endorsement.