Catgut Embedding Therapy for Obesity in Females: Impact on BMI, Waist Circumference, and Quality of Life
This study aims to evaluate the effectiveness of Catgut Embedding Therapy as a treatment for obesity in females, focusing on improvements in body mass index, body weight, hip circumference, and waist circumference.
Catgut embedding group
+ sham catgut embedding group
Treatment Study
Summary
Study start date: January 1, 2014
Actual date on which the first participant was enrolled.This clinical trial focuses on treating obesity in females. It specifically targets those aged between 16 and 65, with a body mass index of 27 or above, and a waist circumference of 80 cm or more. The study explores the therapeutic effects of catgut embedding, a technique where surgical sutures are inserted into specific points on the body. These points, located on the abdomen, have shown potential in managing obesity in previous research. The goal is to understand if this method can improve obesity and enhance the quality of life for these women. During the trial, participants are randomly divided into two groups. One group receives catgut embedding at six acupuncture points on the abdomen, once a week for six weeks. The other group undergoes a sham procedure, mimicking the real one but without actual catgut embedding. The primary outcomes measured are changes in body mass index, waist and hip circumference, and body weight. Additionally, the study evaluates the participants' quality of life using health surveys and questionnaires. Blood tests are also conducted to check lipid profiles, inflammatory markers, and hormones related to obesity. These assessments happen before the treatment begins and after it ends, to determine the effectiveness of catgut embedding in managing obesity.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.90 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.From 20 to 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
ShamStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Branch of Chinese Medicine, Taipei City Hospital
Taipei, TaiwanOpen Branch of Chinese Medicine, Taipei City Hospital in Google Maps