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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04046718
Other study ID # P.T.REC/012/001579_1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 22, 2019
Est. completion date December 29, 2019

Study information

Verified date August 2021
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

sixty female patients suffering from non-alcoholic fatty liver disease were randomly divided into two equal groups group 1 received electroacupuncture stimulation for 6 weeks at special points of stimulation. group 2 was a control group that received nothing without any change in lifestyle and we assed the response of lipid profile post-treatment protocol in both groupes


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 29, 2019
Est. primary completion date November 25, 2019
Accepts healthy volunteers No
Gender Female
Age group 30 Years to 55 Years
Eligibility Inclusion Criteria: non alcoholic fatty liver BMI 30-40 Exclusion Criteria: - Patients with: (Hepatitis C & b any form of seizure

Study Design


Related Conditions & MeSH terms

  • Fatty Liver
  • Fatty Liver , Electroacupuncture, Lipid Profile

Intervention

Device:
electro-acupuncture stimulation
stimulation of acupoints of the liver meridian of lv3 lv14

Locations

Country Name City State
Egypt faculty of physical therapy Cairo university Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ramy Salama Draz

Country where clinical trial is conducted

Egypt, 

References & Publications (1)

Draz RS, Serry ZMH, Rahmy AF, El Bardesi MS, Taha MM. Electroacupuncture Versus Aerobic Interval Training on Liver Functions in Patients with Nonalcoholic Fatty Liver. J Altern Complement Med. 2020 Jan;26(1):51-57. doi: 10.1089/acm.2019.0182. Epub 2019 Oct 29. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary tri-triglycerides (mg/dl) , total cholesterol (mg/dl) , HDL (mg/dl) , LDL (mg/dl) lowering of total lipid profile in study group 6 weeks
Secondary weight (kg) , height (m), BMI (kg/m2) calculation of body mass index 1st week

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