Can smoking sabotage gum grafts? a new trial investigates
NCT ID NCT07777185
First seen Aug 20, 2026 · Last updated Aug 26, 2026 · Updated 3 times
Summary
This study looks at whether smoking changes the tissue in the roof of the mouth where a gum graft is taken, and whether that affects how well the graft covers exposed tooth roots. It will compare 12 smokers with 12 non-smokers, all receiving the same surgical procedure for gum recession. Using ultrasound and tissue analysis, researchers will measure healing and success over three months. The goal is to understand if smoking impairs graft outcomes, which could guide future treatment decisions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Coronally advanced flap with subepithelial connective tissue graft (CAF + CTG), a surgical procedure to cover exposed tooth roots
- What this could lead to
- If smoking is shown to impair graft healing, this could lead to tailored treatment plans and better outcomes for smokers undergoing gum recession surgery.
- What could go wrong
- This is a small, early-stage study with only 24 participants, so results may not apply broadly. Smoking's effects on healing are complex, and the study may not capture all factors.
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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About 24 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Feb 2027
An estimate. End dates often move.
- 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 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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. Aged 18 years or older. 2. Systemically healthy, with no systemic disease that could directly affect status or wound healing. 3. Presence of an isolated facial recession on non-molar maxillary teeth: greater than 2 mm, less than 5 mm (up to a maximum of 5 mm). 4. Recession classified as Cairo Type 1 (RT1 = Miller Class I and II), meaning gingival recession without interproximal attachment loss. 5. No previous soft tissue surgery at the surgical site. 6. Good oral hygiene (full-mouth bleeding on probing below 10%). 7. No soft tissue graft previously harvested from the palatal donor site. 8. Able to comply with all study-related procedures, including attendance at all follow-up visits. Exclusion Criteria: 1. Untreated periodontitis or peri-implantitis. 2. Any systemic disease that could potentially impair wound healing, such as diabetes or connective tissue disorders. 3. Pregnancy or breastfeeding. 4. Previous or concurrent use of medications affecting mucosal healing (e.g., steroids or high-dose anti-inflammatory drugs). 5. Coagulation or bleeding disorders. 6. Cleft palate. 7. Active orthodontic treatment with fixed or removable appliances. 8. A history of malignancy, radiotherapy, or chemotherapy for malignancy within the past 5 years. 9. Antibiotic therapy within the past 6 months. 10. Previous connective tissue graft harvested from the palatal donor site. 11. Any other surgical procedure at the palatal donor or recipient site (e.g., apical resection or crown lengthening).
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Ankara University Faculty of Dentistry
Ankara, Yenimahalle, 06560, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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