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Blood-Derived clot may regrow bone in gum disease

NCT ID NCT07764029

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 13, 2026 · Last updated Aug 14, 2026 · Updated 1 time

Summary

This trial compares two surgical approaches for treating furcation defects—bone loss where tooth roots split—in adults with periodontitis. One group receives a mix of advanced platelet-rich fibrin (A-PRF+) and bone graft material, while the other gets a collagen membrane with the same graft. The study measures gum healing, bone regrowth via 3D imaging, and patient comfort over six months to see if the blood-derived fibrin offers an advantage.

What this could mean

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

Active substance
Advanced platelet-rich fibrin (A-PRF+) combined with bovine xenograft, compared to collagen membrane with xenograft, during periodontal flap surgery.
What this could lead to
If effective, this approach could improve bone and gum healing around molars with furcation defects, potentially saving teeth that might otherwise be lost.
What could go wrong
This is a small early-stage trial, so results may not apply broadly. Surgery carries risks like infection, pain, or incomplete healing, and the A-PRF+ may not outperform the standard collagen membrane.

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

About 22 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2026

Expected to finish

Jun 2027

An estimate. End dates often move.

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

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: * Patients over 18 years old * Patients diagnosed with periodontitis who have completed non-surgical treatment: scaling and root planing * Patients attending a follow-up visit at least 5 weeks after non-surgical treatment, demonstrating compliance and good oral hygiene cooperation * Presence of a mandibular molar with a Degree II furcation involvement according to Hamp (1975), presenting a residual periodontal pocket at the buccal site (PPD ≥ 5mm) after non-surgical treatment, and showing radiolucency in the furcation area on CBCT imaging * Plaque Index (PlI) \< 1 following non-surgical treatment * Width of keratinized gingiva ≥ 2mm * Teeth with furcation defects where gingival recession does not extend apically beyond the buccal furcation fornix (no supragingival furcation exposure) * Teeth without occlusal trauma, pulpal or periapical pathologies, and no combined periodontic-endodontic lesions * Degree II furcation involvement according to Hamp (1975) and Subclass A or B according to Tarnow and Fletcher (1984) * The defect is located apical to the interproximal alveolar bone crest on CBCT imaging Exclusion Criteria: * Patients with systemic diseases affecting periodontal treatment outcomes, such as: diabetes mellitus, heart disease requiring anticoagulant therapy, blood disorders, immunodeficiency, etc * Pregnant or lactating patients * Patients who have used antibiotics or any other medications affecting periodontal treatment outcomes within the last 6 months * Patients who smoke tobacco. * Patients who have used aspirin or medications affecting blood coagulation within 2 weeks prior to the blood collection for PRF preparation * Patients with a history of allergy to local anesthetics * Defects associated with grade II tooth mobility that has not been splinted, or grade III tooth mobility according to Miller (2014)

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Conditions

The condition(s) this trial relates to.

Furcation Defects periodontitis

As listed by the trial registrant

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

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Faculty of Dentistry, University of Medicine and Pharmacy at Ho Chi Minh City

    RECRUITING

    Ho Chi Minh City, Ho Chi Minh City (HCMC), 700000, Vietnam

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