Osteoporosis drug may slow jaw healing after tooth removal
NCT ID NCT01648686
First seen Jun 26, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study looked at 66 postmenopausal women with osteoporosis who were either taking alendronate (a common bone-strengthening drug) or not. Researchers measured how well the jawbone healed after a tooth extraction using X-rays taken right after, then at 30 and 90 days. The goal was to see if alendronate might be a risk factor for slower bone healing in the jaw.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- alendronate
- What this could lead to
- If successful, this could help dentists and doctors better manage tooth extractions in women taking alendronate for osteoporosis.
- What could go wrong
- This is a small, completed observational study, not a treatment trial. It only looks at bone healing after extraction, so it won't change how osteoporosis is treated.
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
-
66 people
The number who actually took part.
- Started
-
Sep 2012
- Finished
-
Nov 2015
- 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
-
45 to 70 years
- Sex
-
Female participants only
- 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 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: * Postmenopausal osteoporotic women * Treated with alendronate per os (70 pg weekly) for BP+ experimental group and untreated with this therapy for the BP * Control group * Subjected to single root tooth extraction- 45 to 70 years of age Exclusion Criteria: * Maxillofacial irradiations * Dental extraction with adjunction of material interfering with bone healing * Severe pathologies inconsistent with this study * Bisphosphonate treatment for BP- control group * Women treated with denosumab (prolia®) * Women already included to an another dental extraction
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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
-
Hotel-Dieu Hospital
Nantes, 44042, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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