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Study of bone augmentation with biodegradable materials

Assessment of the efficacy of biodegradable materials, poly(L-lactic Acid/ipsilon-Caprolactone) membrane and poly(L-lactic-co-glycolic acid) pin for guided bone regeneration - Assessment of the efficacy of biodegradable materials, P(LA/CL) membrane and PLGA pin for GBR

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs032240332
Enrollment
10
Registered
2024-09-12
Start date
2024-09-12
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Severe alveolar bone atrophy

Interventions

use biodegradable pin

Sponsors

Seigo Ohba
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who undergo dental implant treatment and have insufficient alveolar bone volume at the implant placement site and therefore require bone augmentation by GBR prior to implant placement. 2. Age: 20 and older than 20, and younger than 90. 3. Patients who have sufficient explanation about this study and agree to participant in this study by their own decision.

Exclusion criteria

Exclusion criteria: 1. Patients with severe hematological diseases 2. Patients with abnormalities in kidneys, digestive organs, or other calcium-metabolizing organs, or suspected collagen disease 3. Patients who are not expected to visit the hospital at the decided dates. 4. Patients who are not followed the protocol of this study. 5. Patients who smoke 6. Pregnant or lactating patients 7. Patients who can not show their own decision by themselves. 8. Patients who have illnesses which are listed in data sheet. 9. Patients who are not considered to be suitable to join this study by the researchers.

Design outcomes

Primary

MeasureTime frame
efficacy: augmented bone volume according to CBCT images. bone volume was evaluated before, right after, 150 plus/minus 28 days after GBR, and after dental implant placement by CT data.

Secondary

MeasureTime frame
1. safety; adverse event during the study 2, efficacy: Ncm values of implant placement. 3. efficacy: ISQ value after dental implant placement. 4. efficacy: Histological evaluation with bone biopsy.

Contacts

Public ContactOhba Seigo

SHOWA Medical University Dental Hospital

sohba@dent.showa-u.ac.jp+81-3-3787-1151

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026