Clinical Trials Directory

Trials / Completed

CompletedNCT02013596

Transcutaneous Electrical Acupoint Stimulation(TEAS) for Hepatic and Renal Dysfunction After Pneumoperitoneum

Effect of Transcutaneous Electrical Acupoint Stimulation(TEAS) on the Hepatic and Renal Function Impaired by Pneumoperitoneum: a Prospective, Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
168 (actual)
Sponsor
Zhihong LU · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the effect of TEAS pretreatment and treatment on hepatic and renal dysfunction induced by pneumoperitoneum in patients undergoing laparoscopic surgeries.

Detailed description

Patients were randomly assigned to three groups, control group and two intervention groups, receiving TEAS before and after general anesthesia induction respectively. TEAS was given through electrodes attached to acupoints. The time for TEAS was 30min. Venous blood samples were collected before and 20min after pneumoperitoneum. Hepatic and renal function index including AST, ALT, ALP, BUN, Cr were measured.

Conditions

Interventions

TypeNameDescription
OTHERTEAS pretreatmentElectric stimulation was given through electrode attached to specific acupoints for 30mins before anesthesia induction
OTHERTEAS treatmentTranscutaneous Electrical Acupoint Stimulation was given to the patient at the same time of the start of anesthesia induction for 30mins

Timeline

Start date
2013-12-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2013-12-17
Last updated
2016-01-14

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02013596. Inclusion in this directory is not an endorsement.