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Comparison between dental implants placed in bone grafted extracion site and those placed 4-8 weeks after implant placement

Comparative analysis of implant following ridge preservation and early placed implants: randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0004014
Enrollment
18
Registered
2019-05-30
Start date
2016-03-02
Completion date
Unknown
Last updated
2019-06-17

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

Conditions

None listed

Interventions

Procedure/Surgery : Group LP/ARP: late implant placement following ridge preservation -&gt
implant placement after 4 months of healing post alveolar ridge preservation Group EP: early implant placement -&gt
implant placement after 4-8 weeks post-extraction The above two experimental groups are established. The difference of two groups are i) ridge preservation at the time of tooth extraction and ii) hea

Sponsors

Kyung Hee University Dental Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adult aged 20 years old or older 2. Have adequate oral hygiene for implant therapy 3. Have one tooth in either the anterior maxilla or mandible, including incisors, canines and premolars requiring extraction 4. In pre-op radiograph and clinical examination, all socket walls have less than 75% bone loss

Exclusion criteria

Exclusion criteria: 1. Smoking more than 10 cigarettes per day 2. Have uncontrolled systemic diseases such as, diabetes mellitus and hypertension 3. Have untreated periodontal disease 4. Inability to consent for participation in the study 5. In pregnancy 6. Have head and neck radiation 7. Have a medication condition or take medication affecting soft and hard tissue healing, such as bisphosphonate medication, chemotherapeutic and immunosuppressive drug or autoimmune disease. 8. Have alcoholism and drug abusive habit 9. Take part in another clinical trial

Design outcomes

Primary

MeasureTime frame
Change of soft tissue levels

Secondary

MeasureTime frame
patient reported outcome;total cost;change of hard tissue;Pink/White esthetic score;clinical parameters (probing depth, modified plaque score, modified sulcus bleeding index)

Countries

Korea, Republic of

Contacts

Public ContactHYUN-CHANG LIM

Kyung Hee University Dental Hospital

periodent81@gmail.com+82-2-958-9382

Outcome results

None listed

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