Glue instead of heat: a new way to seal varicose veins
NCT ID NCT07827339
First seen Sep 18, 2026 · Last updated Sep 18, 2026
Summary
Researchers are testing a new adhesive system that seals the great saphenous vein in people with varicose veins. The trial compares this adhesive, delivered through a tube, with radiofrequency ablation, a standard treatment that uses heat to close the vein. About 179 adults with varicose veins will be randomly assigned to one of the two treatments. The main goal is to see whether the adhesive closes the vein as completely as the heat treatment, based on ultrasound scans.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a vein closure adhesive delivered through a tube to seal the diseased vein
- What this could lead to
- If it works, the adhesive could offer a treatment that seals varicose veins without the heat and nerve irritation that radiofrequency ablation can cause.
- What could go wrong
- The trial is relatively small and compares the adhesive only against one standard treatment. The adhesive may fail to close the vein completely, or it may cause reactions that heat-based treatment avoids.
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
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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
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179 people
The number who actually took part.
- Started
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Oct 2023
- Finished
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Apr 2026
- Lead sponsor
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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
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥ 18 years and ≤ 80 years at the time of screening, no restrictions on gender. 2. Clinical diagnosis of unilateral / bilateral varicose GSV of lower extremities. This operation only deals with unilateral trunk of GSV. 3. CEAP classification of C2 - C4b. 4. Ability to understand the requirements of the study, provide informed consent, and attend follow-up visits. Exclusion Criteria: 1. Life expectancy \<1 year. 2. Patients with vessel diameter \< 3mm or \> 12mm in the target segment of the GSV. 3. Deep vein thrombosis (DVT) (excluding intermuscular venous thrombosis) or pulmonary embolism (PE). 4. Undergone interventional or surgical treatment of the GSV in the target limb. 5. Allergies to lidocaine or cyanoacrylates. 6. GSV was extreme distorted and thus unsuitable for minimally invasive interventional treatment. 7. Aneurysm of the target vein with local vein diameter \>12 mm. 8. Active superficial thrombophlebitis in the target GSV. 9. Pregnant and / or lactating patients. 10. Patients who are participating in clinical trials of other drugs or medical devices. 11. Patients considered ineligible for inclusion by the investigator.
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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
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Hangzhou First People's Hospital
Hangzhou, Zhejiang, 310006, China
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Ruian People's Hospital
Ruian, Zhejiang, 325200, China
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Shanxi Bethune Hospital
Taiyuan, Shanxi, 030032, China
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Suzhou Municipal Hospital
Suzhou, Jiangsu, 215002, China
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The Affiliated Hospital of Qingdao University
Qingdao, Shandong, 266000, China
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The Fourth Affiliated Hospital, Zhejiang University School of Medicine
Jinhua, Zhejiang, 322000, China
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