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Abdominal ObesityNCT07125716

Suture Length Effects in Acupoint Implantation for Abdominal Obesity

A study testing 1 inch and 0.5 inch in people with Abdominal Obesity and Obesity, run by Chang Gung Memorial Hospital at 1 site in Taiwan.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

Obesity is a metabolic disorder and has become a global health issue with a steadily increasing prevalence. According to the Health Promotion Administration's statistical report, the overweight and obesity rate among adults in Taiwan was 50.3% between 2017 and 2020. Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Abdominal Obesity, Obesity
What is being tested?
1 inch and 0.5 inch
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
78 participants
Where
1 siteTaiwan
Study dates
1 Aug 2025to 31 Jul 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Willing to sign a written informed consent form
  • BMI ≥27 kg/m² (Ministry of Health and Welfare standard)
  • Waist circumference ≥90 cm for men
  • Waist circumference ≥80 cm for women
  • Age between 18 and 65 years

Who cannot join

  • Endocrine disorders (thyroid disease, pituitary disorders, and diabetes)
  • Autoimmune diseases (systemic lupus erythematosus, Sjögren's syndrome, and rheumatoid arthritis)
  • Heart diseases (heart failure, arrhythmia, etc.)
  • Abnormal liver function
  • Abnormal kidney function
  • Stroke within the past year
Show all 11Show fewer
  • Pregnant or breastfeeding women
  • Coagulation disorders
  • Tumors
  • Participation in weight loss treatment within the past 6 months
  • Any other condition deemed unsuitable for the trial by the physician

Trial locations and contacts

1 site in 1 country.

Taiwan1 site
  • Chang-Geng Medical Foundation Keelung Chang-Geng Memorial Hospital

    Keelung

Other trials in Taiwan

About this study

Official title: Effects of Different Lengths of Surgical Sutures in Acupoint Catgut Implantation on Simple Abdominal Obesity in Adults

Obesity is a metabolic disorder and has become a global health issue with a steadily increasing prevalence. According to the Health Promotion Administration's statistical report, the overweight and obesity rate among adults in Taiwan was 50.3% between 2017 and 2020. Based on the Ministry of Health and Welfare's criteria, a BMI ≥27 kg/m² is classified as obese.

Studies have shown that acupuncture can effectively reduce body weight with low cost and minimal side effects. Acupoint catgut embedding is a treatment method that combines traditional meridian acupuncture with modern medical materials by implanting surgical sutures into acupoints to provide continuous stimulation.

Read more

A 2022 systematic review found that catgut embedding is more effective than traditional acupuncture, requires fewer treatment sessions, and has a high safety profile. However, no studies have yet investigated whether different lengths of implanted surgical sutures affect treatment outcomes.

This study is a single-center, double-blind, randomized controlled trial aimed at identifying the optimal suture length for acupoint catgut embedding, in order to enhance its efficiency and therapeutic effect.

Being tested
1 inch, 0.5 inch
Medical subject headings
Obesity, Abdominal, Obesity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • 1 inchDevice

    1 inch suture length

  • 0.5 inchDevice

    0.5 inch suture length

Study groups in NCT07125716
Study groupRoleWhat they receive
1 inch suture lengthExperimentalNot described
Receives: Device: 1 inch
0.5 inch suture lengthActive comparatorNot described
Receives: Device: 0.5 inch

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Waist circumference

    Measured: 1 week,4 week,8 week

Secondary outcomes (5)
  1. hip circumference

    Measured: 1 week,4 week,8 week

  2. weight

    Measured: 1 week,4 week,8 week

  3. BMI

    Measured: 1 week,4 week,8 week

  4. VAS

    Measured: 1 week,4 week,8 week

  5. Ultrasound Fat Thickness

    Measured: 1 week,4 week,8 week

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Aug 2025
  2. Study start1 Aug 2025
  3. Primary completion30 Jun 2026 (estimated)
  4. Study completion31 Jul 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Care provider
Enrolment
78 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07125716
Sponsor's protocol ID
202500161A3
Status last verified
Apr 2025
First submitted
10 Aug 2025
Last updated
15 Aug 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing 1 inch and 0.5 inch in people with Abdominal Obesity and Obesity, run by Chang Gung Memorial Hospital at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 15 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Waist circumference (time frame: 1 week,4 week,8 week). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Aug 2025.

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