Bone Healing After Dental Extraction in Postmenopausal Osteoporotic Women Treated With Alendronate Per os Weekly

NCT ID: NCT01648686

Last Updated: 2025-09-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 66 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-09-19
• Study Completion Date: 2015-11-05

Brief Summary

The purpose of this study is to determine whether the oral alendronate treatment of post-menopausal osteoporosis could be a risk factor for jaw bone healing after dental extraction.

Detailed Description

Alendronate is the main oral bisphosphonate used in the treatment and the prevention of the postmenopausal osteoporosis because of its high antiresorbant ability for bone tissue. Alendronate delayed bone healing after dental extraction on animals models, murine as canine. Anti-angiogenic and anti-osteoclastic characteristics are suggested to explain this phenomenon. There is no available data in human and it is now well known that bisphosphonates are involved in the occurrence of osteonecrosis of the jaws even if this major adverse effect seems to be very seldom with oral alendronate. Moreover, bisphosphonate showed toxicity for oral mucosal cells. The main aim of this study is to quantify the impact of oral alendronate weekly treatment on bone and mucosa healing after dental extraction in postmenopausal osteoporotic women. A secondary aim is to investigate a panel of 50 peptids potentially involved in bone and mucosal healing and to detect changes in their rates by salivary proteomic approach. The investigators hope so identify salivary biomarkers of bone and/or mucosa healing in these women.

Our hypothesis is that after dental extraction, bone healing could be delayed in postmenopausal osteoporotic women treated with oral weekly alendronate (BP+ group) versus matched osteoporotic women untreated with bisphosphonates (BP- group).

This is a prospective and multicentric (17 investigation centers dispatched in France) study including 140 osteoporotic postmenopausal women treated weekly with oral bisphosphonates (BP+ group) and 140 osteoporotic postmenopausal women untreated with bisphosphonates (BP- group). This is a clinical follow-up study (T0, T0 + 7, T0 + 30, T0 + 90 days), a radiological study (T0, T0 + 30, T0 + 90 days), and a salivary proteomic study (T0, T0 + 30, T0 + 90 days). This is a 4 years study starting in april 2012 (anticipated date).

The main investigated parameters are:

• Bone healing: Bone filling rate (in %) of the post-extractional alveolar socket (BFR) at T0, T0 + 30 and T0 + 90 days by a radiographic approach.
• Mucosa healing: mucosal injury by metric approach at T0 and T0 + 30 days.
• Salivary biomarkers: Fifty peptides by proteomic approach at T0 and T0 + 30 days;

The investigators expect that this study will allow us to build a reference scale of bone and mucosa healing in osteoporotic postmenopausal women treated weekly by oral alendronate. This scale will be a helpful tool for dental physicians. The investigators hope also to identify salivary biomarkers variations to make a diagnosis and a prognosis tool of worse bone healing in these patients.

Perspectives of this study is to constitute a national network of deleterious effect on bone healing in such women patients and to up-date guidelines in this area.

Conditions

Alveolar Bone Healing After Dental Extraction

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SCREENING
• Blinding Strategy: NONE

Study Groups

Women treated by bisphosphonate

Postmenopausal osteoporotic women treated by alendronate 70 mg weekly per os

Group Type: ACTIVE_COMPARATOR

Dental extraction

Intervention Type: PROCEDURE

3 dental radiographies realised immediately, then 30 days, then 90 days after dental extraction

Women didn't treat by bisphosphonate

Postmenopausal osteoporotic women untreated by bisphosphonates

Group Type: SHAM_COMPARATOR

Dental extraction

Intervention Type: PROCEDURE

3 dental radiographies realised immediately, then 30 days, then 90 days after dental extraction

Interventions

Dental extraction

3 dental radiographies realised immediately, then 30 days, then 90 days after dental extraction

Intervention Type: PROCEDURE

Eligibility Criteria

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

• Minimum Eligible Age: 45 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

URC-CIC Paris Descartes Necker Cochin

OTHER

Sponsor Role: collaborator

Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Christian ROUX, MD, PhD

Role: STUDY_CHAIR

Hôpital Cochin

Locations

Hotel-Dieu Hospital

Nantes, , France

Countries

France

References

Lesclous P, Cloitre A, Catros S, Devoize L, Louvet B, Chatel C, Foissac F, Roux C. Alendronate or Zoledronic acid do not impair wound healing after tooth extraction in postmenopausal women with osteoporosis. Bone. 2020 Aug;137:115412. doi: 10.1016/j.bone.2020.115412. Epub 2020 May 20.

Reference Type: BACKGROUND

PMID: 32404281 (View on PubMed)

Other Identifiers

P110126

Identifier Type: -

Identifier Source: org_study_id