Acupuncture-Like needles may ease pain after stomach procedure
NCT ID NCT06828250
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether placing tiny needles under the skin (intradermal needle therapy) can reduce pain after a stomach procedure called endoscopic submucosal dissection (ESD). 76 patients were randomly assigned to receive either standard care or standard care plus the needle therapy. Researchers tracked pain levels, medication use, and side effects for 72 hours after surgery. The goal is to find a safe, non-drug way to manage post-surgery pain.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- intradermal needle therapy (acupuncture-like device)
- What this could lead to
- If it works, this could offer a simple, drug-free way to manage pain after stomach surgery.
- What could go wrong
- This is a small, completed study with only 76 participants. The results may not apply to everyone, and the therapy may not be more effective than standard care.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
76 people
The number who actually took part.
- Started
-
Mar 2025
- Finished
-
Jun 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: All patients who signed informed consent after gastric ESD were enrolled in this study. Exclusion Criteria: 1. Patients who pulled out the needles in advance; 2. Individuals with psychiatric disorders, impaired communication abilities, or difficulties in self-assessment of pain.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
The First Hospital of Lanzhou University
Lanzhou, China
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