Evaluation of various substitutes for management of extraction socket

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002872

Enrollment

Registered

2018-05-17

Start date

2016-05-31

Completion date

Unknown

Last updated

2019-03-11

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 : In the control group, the socket was allowed to heal naturally. In the test group, the socket was filled with freeze-dried irradiated allogenic bone (ICB Cortical®, Rocky Mountain Tis

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (i) type 3 or 4 extraction socket morphology (= 3 mm of hard tissue loss in 1 or more socket walls) according to published extraction socket classification (Caplanis N, et al. Extraction defect assessment, classification, and management. J Calif Dent Assoc 2005; 33: 853-863), (ii) no systemic disease contraindicating surgical procedures or compromising wound healing, and, (iii) clinically healthy periodontal status or treated/well-managed periodontal disease (bleeding on probing and plaque index < 25%)

Exclusion criteria

Exclusion criteria: (i) current smoker (= 10 cigarettes per day), (ii) pregnancy or lactation, (iii) uncontrolled or untreated periodontal disease, and (iv) inability to understand the trial purpose and provide informed consent.

Design outcomes

Primary

Measure	Time frame
Cone beam CT analysis	—

Secondary

Measure	Time frame
Histormorphometric analysis;Need of additional bone graft	—

Countries

Korea, Republic of

Contacts

Public ContactDong-Woon Lee

VHS Medical Center

dongden@daum.net+82-2-2225-1928

Outcome results