Mouthrinse showdown: which rinse heals gum grafts best?

NCT ID NCT07689695

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 08, 2026 · Last updated Jul 09, 2026 · Updated 1 time

Summary

This trial tests three mouthrinses—hypochlorous acid, hyaluronic acid, and chlorhexidine—to see which helps the palate heal best after a gum graft. Fifty-four adults having gum graft surgery will rinse with one of the three solutions for 14 days. Researchers will check wound healing, pain, and bleeding over 28 days to find the most effective rinse for recovery.

What this could mean

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

Active substance
Hypochlorous acid, hyaluronic acid, and chlorhexidine mouthrinses
What this could lead to
If one mouthrinse proves superior, it could improve healing and reduce pain after gum graft surgery, making recovery more comfortable.
What could go wrong
This is a small, early-stage trial (54 participants) comparing existing products, so results may not apply to everyone. Any mouthrinse might cause irritation or not speed healing as hoped.

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

54 people

The number who actually took part.

Started

Jun 2020

Finished

Jul 2021

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 to 55 years

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 between 18 and 55 years. * Indication for free gingival graft surgery to increase keratinized tissue width. * Systemically healthy individuals. * Palatal donor site suitable for graft harvesting. * No history of periodontal surgery within the previous six months. * Ability and willingness to comply with postoperative instructions and follow-up visits. * Provision of written informed consent. Exclusion Criteria: * Systemic diseases that could affect wound healing. * Smoking. * Antibiotic use within the previous six months. * Pregnancy or lactation. * Known hypersensitivity to chlorhexidine, hypochlorous acid, hyaluronic acid, or any component of the study products. * Active oral infection, periodontal abscess, or poor oral hygiene. * Previous palatal surgery, mucosal lesions, anatomical limitations, or conditions affecting hemostasis at the donor site. * Inability or unwillingness to comply with the study protocol.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Van Yuzuncu Yil University Faculty of Dentistry

    Van, Tuşba, 65100, Turkey (Türkiye)

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