N/A
Completed N=120
Impact of Treatment With ALVEOGYL in Patients With Post-extraction Dry Socket
Dry Socket
Source: ClinicalTrials.gov NCT05536115 ↗
Enrolled (actual)
120
Serious AEs
0.0%
Results posted
Feb 2026
Primary outcomePrimary: Pain Using a Visual Analog Scale (VAS : 0-10) — 106; 4 Participants
Summary
Alveogyl (Septodont, Saint-Maur-des-Fossés - France) is a Medical Device used as dressing in case of dry socket.
ALVE study is a clinical investigation measuring Alveogyl performance and safety in patients with post-extraction dry socket.
The study takes place in India and in France where Alveogyl is already marketed, since 2010 in France and since 2014 in India .
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Pain Using a Visual Analog Scale (VAS : 0-10) |
106; 4 | — |
| SECONDARY Analgesic Use |
63; 47; 20; 90 | — |
| SECONDARY Healing of the Alveolar Mucosa |
4.0 | — |
| SECONDARY Signs of Local Inflammation |
19; 91 | — |
| SECONDARY Antiseptic Effect |
12; 96; 2; 2; 108; 0 | — |
| SECONDARY Hemostasis |
96; 13; 1; 0; 110; 0 | — |
| SECONDARY Complication Rate |
0; 110 | — |
Eligibility Criteria
Inclusion Criteria
- Male or female patient, adult or child
- Positive diagnosis of dry socket occurring after the extraction of a permanent tooth (mature or immature)
- Signed informed consent
- In France only : Patient affiliated to a Health Insurance Scheme ("sécurité sociale")
Exclusion Criteria
- Spreading infection in the alveolar socket
- Placement of Alveogyl done immediately after tooth extraction
- Multiple post-extraction dry sockets
- Patient treated with cervico-facial radiotherapy
- Immunodeficiency related to any diseases or current treatments
- Psychiatric patient or patient unable to assess his/her pain via the study Pain VAS
- Patient with history of hypersensitivity to one of the components
- Patient on post extraction of deciduous teeth
- Participation in another clinical investigation
Data sourced from ClinicalTrials.gov (NCT05536115). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.