ClinicalTrials.gg
Status unknownNCT03325179Updated Oct 30, 2017

A Clinical Trial of Thread-embedding Therapy at Acupuncture Point for Simple Obesity

An interventional study of Thread-embedding Therapy in Weight Loss and Simple Obesity, sponsored by Shanghai University of Traditional Chinese Medicine. Status unknown at 1 site in China. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-10-30.

Sponsored by Shanghai University of Traditional Chinese Medicine · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jun 2017), so the status shown — last known as Recruiting — may be out of date.

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled Jan 2017, registered Sep 2017).
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Not applicable
Ages
18 Years to 60 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 51 studies in Weight Loss with a site in China — 26 open to participants now, 27 under way, 6 of them phase 3. Weight Loss · China.

Planned enrollment
24th of 46
100 · median 103
Started
2017
with 1 other
No phase
26 of 51
12 open now
Registered
5th of 51
by date

Among the 51 studies in Weight Loss with a site in China, this one is the 24th largest by planned enrollment of the 46 interventional ones that give a count, is one of 2 that started in 2017, is one of 26 with no phase, and was the 5th registered.

Weight Loss

1,815 studies on the registry are indexed under Weight Loss; 294 are open to participants now.

Browse Weight Loss studies →

Open to participants now

26 of the 51 studies in Weight Loss with a site in China are open now. Recruiting first, the newest first:

21 more — sign in →

All 26 open studies →

A study can be open while its sites in China have not opened yet or have stopped. Only those recruiting at a site in China →

Who these studies take

Of the 196 Weight Loss studies recruiting now, 71 (36%) set no upper age limit and 108 (55%) stop at 75 or younger; 21 take children under 18; 58 take healthy volunteers.

This study: 18 Years to 60 Years · all sexes · healthy volunteers too.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

Was this useful?
Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 51 studies in Weight Loss with a site in China, or all of them as a file.
02

Study summary

Thread-embedding Therapy has been used for treating Obesity in recent years. This research is aimed to observe the clinical effect of thread-embedding therapy in treating Simple Obesity. One hundred patients is planned to be enrolled in the research and receive a thread-embedding therapy. The level of BMI, serum triglyceride, cholesterol and fasting blood glucose will be adopted for evaluation before and after therapy.

Read the detailed description

Each participant will receive thread-embedding therapy every two weeks, and eight times in all.Blood test will be taken at the beginning of the first week of the whole therapy, and at the end of the 8th therapy. During the periods of whole therapy, the participants shall follow diets control and physical exercise as the protocol described.

03

Conditions studied

  • Weight Loss
  • Simple Obesity

Browse trials for

Keywords

  • Simple Obesity
  • Thread-embedding Therapy
  • Acupuncture
04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • patients with age from 18 to 60 years old;
  • patients with ≥ 24, meanwhile waist more than 85 cm (for male) or 80 cm (for female);
  • patients with diagnosed as central adiposity and/or Simple obesity according to the diagnosis criteria;
  • patients who is willing to cooperate with the test treatment and signed .

Exclusion criteria

Exclusion Criteria:

  • Pregnant or lactating women;
  • patients who Syncope after acupuncture;
  • patients who present reactions after acupoint-embedding therapy;
  • patients with serious heart, liver, kidney, brain and other diseases;
  • patients with severe primary diseases;
  • patients with psychiatric diseases;
  • patients who did not meet the criteria for the inclusion criteria while investigators find out during the trial;
  • participants who did not complete dietary control and physical exercise as the protocol described.
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    participants received treatment

    100 participants who are diagnosed as simple obesity under the standards of... are planned to enrolled in the trial. Each will receive Thread-embedding therapy.

    Other: Thread-embedding Therapy

Interventions

  • OtherThread-embedding Therapy
06

What researchers measure

Primary outcomes

  1. The change Body Weight

    a 5 percent of loss of body weight will be judged as effective

    Time frame: participants will receive Thread-embedding Therapy twice a week lasting for 16 weeks subsequently.8 times in all.

Secondary outcomes

  1. The effection on cholesterol

    a target examined by blood test, in order to compare the Lipid metabolism

    Time frame: Therapy is the same as mentioned above. Participants will take blood test at the beginning of the first week of the therapy, and at the end of the 16th week.

  2. The effection on triglyceride

    a target examined by blood test, in order to compare the Lipid metabolism

    Time frame: Therapy is the same as mentioned above. Participants will take blood test at the beginning of the first week of the therapy, and at the end of the 16th week.

  3. The effection on fasting blood glucose

    to compare the level of glucose in order to get the message of improvement of blood glucose disorder by our therapy.

    Time frame: Therapy is the same as mentioned above. Participants will take blood test at the beginning of the first week of the therapy, and at the end of the 16th week.

07

Study locations

1 of 1 sites recruiting
  • Institute of Digestive Diseases of Longhua Hospital affiliate to Shanghai University of Traditional Chinese Medicine
    Shanghai, Shanghai 200032, China
    Recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jan 2017 (actual). Primary completion is estimated for Dec 2017, 11 months after the start.

Of 670 non-industry interventional studies with no phase under Weight Loss, half reached primary completion within 25 months of starting (the median), counting those still running; a quarter within 13 and three quarters within 45. This study's planned 11 months is below that.

Counting every sponsor, half of 729 studies reached it within 24 months; a quarter within 11 and three quarters within 43.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 3, 2017
First posted
Oct 30, 2017
StartActual
Jan 3, 2017
Primary completionEst.
Dec 31, 2017
CompletionEst.
Mar 31, 2018
Last update
Oct 30, 2017
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Oct 30, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03325179
Responsible party
Sponsor
First posted
Oct 30, 2017
Start date
Jan 3, 2017
Primary completion
Dec 31, 2017 (estimated)
Completion
Mar 31, 2018 (estimated)
Last update
Oct 30, 2017

Study contacts

Miao Wang
Contact
wangmiao_126@126.com
+86-64385700 ext. 9507

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2017. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion