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Comparison of sticky bone and particulate bone in the extraction socket preservation : A Randomized Controlled Clinical Trial

Comparison of sticky bone and particulate bone in the extraction socket preservation : A Randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0009560
Enrollment
40
Registered
2024-06-21
Start date
2021-10-08
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

None listed

Interventions

Medical Device : Xenogeneic bone substitutes were used to fill sockets after tooth extraction. The xenogeneic bone substitutes included moldable and customizable bovine bone mineral (S1, MedPark, Busa

Sponsors

Yonsei University Health System, Dental Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: aged = 18 years and = 65 years; one tooth requiring extraction, prospectively scheduled for implant placement 4-6 months after the extraction; all extraction sites had adjacent teeth; presence of four-wall or three-wall sockets of teeth recommended for extraction due to endodontic failure, caries, or root fracture, which required ridge preservation following tooth extraction; no possibility of plans to become pregnant.

Exclusion criteria

Exclusion criteria: Maxillary and mandibular second or third molars; smoking >10 cigarettes per day; uncontrolled diabetes or hypertension; soft tissue transplant surgery at the tooth extraction site undergone within the previous 6 months; long-term steroid or nonsteroidal anti-inflammatory drug therapy; history of intravenous or oral rheumatism medication; history of intravenous or oral bisphosphonate treatment for more than 3 months; presence or history of osteonecrosis of the jaws or bone diseases such as cysts and tumors; radiation or chemotherapy treatment completed within the previous 5 years; known allergy to any material or medication used in the study; poor oral hygiene; an acute infection (abscess) or presence of pus in or close to the site intended for extraction; mental or psychiatric disorder; pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
Changes in ridge height and width

Secondary

MeasureTime frame
percentage of new bone area (%NBA); percentage of residual material area(%RMA); percentage of connective tissue area (%CTA)

Countries

Korea, Republic of

Contacts

Public ContactYiseul Choi

Yonsei University Health System, Dental Hospital

loa@yuhs.ac+82-2-2228-8978

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026