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Can a gel and a mesh stop Post-Surgery neck adhesions?

NCT ID NCT05851560

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This study tested whether applying oxidized regenerated cellulose and hyaluronic acid during thyroid surgery can prevent painful adhesions that often form after the procedure. 45 adults with benign goiter or thyroid cancer were enrolled. The goal was to see if these barriers reduce neck discomfort, swallowing problems, and skin sticking to the trachea.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
oxidized regenerated cellulose and hyaluronic acid
What this could lead to
If it works, this could provide a safe way to reduce neck discomfort, swallowing difficulty, and skin sticking after thyroid surgery.
What could go wrong
This is a small, early-phase trial with only 45 participants, so results may not apply broadly. The anti-adhesion effect is still uncertain.

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

Phase 1

The first testing in people. Mainly checks safety and dose, usually in a small group.

Participants

45 people

The number who actually took part.

Started

May 2023

Finished

Aug 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

20 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age more than 20 years of age. * Patients diagnosed with benign goiter or thyroid cancer that will undergo open thyroidectomy (either unilateral or bilateral total thyroidectomy with or without central lymph node dissection). * Naïve patients to thyroid surgery. * Subjects are willing to comply with all aspects of the study and have signed informed consent form. Exclusion Criteria: * Pregnant or lactating female patients. * Presence of severe and uncontrolled illness such as stroke, hypertension, diabetes, chronic renal failure, coagulopathy. * Concurrent diseases/conditions which will be unable to evaluate the outcomes. * Patients with previous neck radiotherapy within 1 year. * Patients receiving any adhesion prevention adjuvant. * Previous history of Keloid or hypertrophic scar. * Participate are hypersensitive to anti-adhesion agents. * Participate in another clinical trial within 1 month. * Participate have drug or alcohol abuse. * Patients' presence of surgical site infection or uncontrolled bleeding. * Anticoagulant used within a week from surger

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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

  • National Taiwan University Hospital

    Taipei, 100229, Taiwan

More trials for these conditions

Other studies related to the condition(s) this trial covers.