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

Z

Zhihong LU

Status

Completed

Conditions

Hepatic Dysfunction Transient
Renal Function Disorder

Treatments

Other: TEAS pretreatment
Other: TEAS treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT02013596
XJH-A-2013-08-2

Details and patient eligibility

About

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.

Full 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.

Enrollment

168 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age>18yrs,<60yrs;
  • ASA 1-2;
  • Scheduled for laparoscopic surgery under general anesthesia;
  • Informed consented

Exclusion criteria

  • Patients with hepatic or renal dysfunction;
  • Patients with severe hypertension or cardiac dysfunction;
  • Patients with severe pulmonary disease;
  • Patients with hemoglobin<100g/L

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

168 participants in 3 patient groups

Control
No Intervention group
Description:
Patients were given no TEAS
TEAS Pretreatment
Experimental group
Description:
Patients were given 30min of TEAS before pneumoperitoneum
Treatment:
Other: TEAS pretreatment
TEAS Treatment
Experimental group
Description:
Patients were given 30min of TEAS during pneumoperitoneum
Treatment:
Other: TEAS treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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