- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05623930
Liver Enzymes and Metabolic Risk Factors Response to Laser Acupuncture Versus Cupping Therapy in Fatty Liver
November 18, 2022 updated by: Ali Mohamed Ali ismail, Cairo University
Hepatic Enzymes and Metabolic-Risk Factors Responses to Laser Acupuncture Versus Cupping Therapy in Fatty Liver
fatty liver disease is characterized by low antioxidants, disturbed lipid metabolism, cardioautonomic functions, and elevated blood measures (glucose, inflammatory markers, liver enzymes)
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
In fatty liver patients,applied cupping (with scarification) will be compared, regarding its effect on antioxidant, lipid metabolism, cardioautonomic functions, and blood measures (glucose, inflammatory markers, liver enzymes), to application of laser on acupoints
Study Type
Interventional
Enrollment (Anticipated)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ali Ismail, lecturer
- Phone Number: 02 01005154209
- Email: ali.mohamed@pt.cu.edu.eg
Study Contact Backup
- Name: ahmed Elfahl, Lecturer
- Email: ahmed.elfahl@buc.edu.eg
Study Locations
-
-
-
Giza, Egypt
- Recruiting
- Cairo Unoversity
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
35 years to 55 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- fatty liver obese patients
Exclusion Criteria:
thoracic diseases heart diseases kidney diseases
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: laser on acupuncture points
In fatty liver diseased patients which their number will be 30 patients, a 3-session/week application of 2-minute laser (for 3 months) on acupoint number 25,40,36 of stomach meridian, acupoints number 3 and 14 of liver meridian, acupoint number 6 of spleen meridian,acupoint number 9.12,4 of conception vessel meridian, acupoint number 14 of governor vessel meridian, acupoint number 4, 11 of large intestine meridian, acupoint number 34 of gall bladder meridian
|
In fatty liver diseased patients which their number will be 30 patients, a 3-session/week application of 2-minute laser (for 3 months) on acupoint number 25,40,36 of stomach meridian, acupoints number 3 and 14 of liver meridian, acupoint number 6 of spleen meridian,acupoint number 9.12,4 of conception vessel meridian, acupoint number 14 of governor vessel meridian, acupoint number 4, 11 of large intestine meridian, acupoint number 34 of gall bladder meridian
|
Active Comparator: cupping (with scarification)
in this fatty liver diseased patients which their number will be 30, cupping (with scarification) or wet cupping will be applied at the first day and the day number 14 in the month for three successive months.
cupping (with scarification) or wet cupping will be applied on urinary bladder acupoint 17 (on the both sides) and governosal vessels acupoints 12,13,and 14.
|
in this fatty liver diseased patients which their number will be 30, cupping (with scarification) or wet cupping will be applied at the first day and the day number 14 in the month for three successive months.
cupping (with scarification) or wet cupping will be applied on urinary bladder acupoint 17 (on the both sides) and governosal vessels acupoints 12,13,and 14.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
high density lipoprotein
Time Frame: 12 weeks
|
it is a component of lipid profile
|
12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
systolic blood pressure
Time Frame: 12 weeks
|
it will be measured by sphygmomanometer
|
12 weeks
|
diastolic blood pressure
Time Frame: 12 weeks
|
it will be measured by sphygmomanometer
|
12 weeks
|
cholesterol
Time Frame: 12 weeks
|
it is a component of lipid profile
|
12 weeks
|
low density lipoprotein
Time Frame: 12 weeks
|
it is a component of lipid profile
|
12 weeks
|
triglycerides
Time Frame: 12 weeks
|
it is a component of lipid profile
|
12 weeks
|
blood glucose
Time Frame: 12 weeks
|
fasting level of blood glucose will be measured
|
12 weeks
|
C reactive protein
Time Frame: 12 weeks
|
high sensitivity levels C reactive protein will be measured
|
12 weeks
|
Malondialdehyde
Time Frame: 12 weeks
|
it ts oxidative stress marker
|
12 weeks
|
aspartate transaminase
Time Frame: 12 weeks
|
it is a hepatic enzyme that reports the functions of liver
|
12 weeks
|
alanine transaminase
Time Frame: 12 weeks
|
it is a hepatic enzyme that reports the functions of liver
|
12 weeks
|
pulse rate
Time Frame: 12 weeks
|
it will be measured manually
|
12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 12, 2022
Primary Completion (Anticipated)
April 1, 2023
Study Completion (Anticipated)
April 1, 2023
Study Registration Dates
First Submitted
November 14, 2022
First Submitted That Met QC Criteria
November 18, 2022
First Posted (Actual)
November 21, 2022
Study Record Updates
Last Update Posted (Actual)
November 21, 2022
Last Update Submitted That Met QC Criteria
November 18, 2022
Last Verified
November 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/004116
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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