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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03806608
Other study ID # Baoxin Huang Depth
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date April 17, 2019
Est. completion date May 2026

Study information

Verified date April 2022
Source Sun Yat-sen University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this randomized controlled trial is to evaluate changes in marginal bone levels and soft tissue dimensions around implants placed with the IAI at different positions in relation to the alveolar crest


Description:

The objective of this randomized controlled trial is to evaluate changes in marginal bone levels and soft tissue dimensions around implants placed with the IAI at different positions in relation to the alveolar crest. Subjects will be included with the absence of 2-4 teeth in the posterior region of the maxilla or mandibular. Twenty patients will be recruited. Two implant placement depths, equicrestal and subcrestal, were randomly assigned to two sites of each patient with a predefined randomization tables (one crestal implant and one subcrestal implant). Patients will be recalled for oral hygiene maintenance and prosthetic controls at 1year, 3 years, 5 years after final restoration.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 20
Est. completion date May 2026
Est. primary completion date May 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: 1. Absence of 2-4 teeth in the posterior region of the maxilla or mandibular; 2. Bone volume sufficient for implants with 4.1-mm size and 8- to 12-mm height and with no need for hard or soft tissue augmentation for implant treatment; 3. Periodontally healthy. Exclusion Criteria: 1. Systemic diseases that may affect bone and soft tissue healing, such as diabetes, osteoporosis, Paget's disease, and patients with cancer; 2. Uncontrolled periodontal disease or poor oral health with neither good nor adequate plaque control; 3. Parafunctional habits, such as the grinding or clenching of teeth; 4. Smoking habit (more than 10 cigarettes per day); 5. Pregnancy and breastfeeding.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Crestal
Subjects will be included with the absence of 2-4 teeth in the posterior region of the maxilla or mandibular. Twenty patients will be recruited. Two implant placement depths, equicrestal and subcrestal, were randomly assigned to two sites of each patient with a predefined randomization tables (one crestal implant and one subcrestal implant).
Subcrestal
Subjects will be included with the absence of 2-4 teeth in the posterior region of the maxilla or mandibular. Twenty patients will be recruited. Two implant placement depths, equicrestal and subcrestal, were randomly assigned to two sites of each patient with a predefined randomization tables (one crestal implant and one subcrestal implant).

Locations

Country Name City State
China Guanghua School of Stomatology,Hospital of Stomatology,Sun Yat-Sen University Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Sun Yat-sen University

Country where clinical trial is conducted

China, 

References & Publications (4)

Huang B, Meng H, Piao M, Xu L, Zhang L, Zhu W. Influence of placement depth on bone remodeling around tapered internal connection implant: a clinical and radiographic study in dogs. J Periodontol. 2012 Sep;83(9):1164-71. doi: 10.1902/jop.2012.110617. Epub 2012 Jan 5. — View Citation

Huang B, Meng H, Zhu W, Witek L, Tovar N, Coelho PG. Influence of placement depth on bone remodeling around tapered internal connection implants: a histologic study in dogs. Clin Oral Implants Res. 2015 Aug;26(8):942-949. doi: 10.1111/clr.12384. Epub 2014 Apr 10. — View Citation

Koutouzis T, Neiva R, Nonhoff J, Lundgren T. Placement of implants with platform-switched Morse taper connections with the implant-abutment interface at different levels in relation to the alveolar crest: a short-term (1-year) randomized prospective controlled clinical trial. Int J Oral Maxillofac Implants. 2013 Nov-Dec;28(6):1553-63. doi: 10.11607/jomi.3184. — View Citation

Valles C, Rodríguez-Ciurana X, Clementini M, Baglivo M, Paniagua B, Nart J. Influence of subcrestal implant placement compared with equicrestal position on the peri-implant hard and soft tissues around platform-switched implants: a systematic review and meta-analysis. Clin Oral Investig. 2018 Mar;22(2):555-570. doi: 10.1007/s00784-017-2301-1. Epub 2018 Jan 8. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Marginal bone loss(MBL) Baseline will be recorded at the time of implantation. Margin bone loss(MBL) will be recorded at 0 day, 4 months, 1 year and 3 years after implant placement. Change from baseline up to 5 years after implantation
Secondary Cumulative survival rate (CSR) Cumulative survival rate will be assessed at final restoration, 1 year, 3 years, 5 years after final restoration Up to 5 years after final restoration
Secondary Pocket probing depth (PPD) Pocket probing depth will be assessed at 1 year, 3 years, 5 years after final restoration Up to 5 years after final restoration
Secondary Plaque index (PI) Plaque index will be assessed at 1 year, 3 years, 5 years after final restoration Up to 5 years after final restoration
Secondary Bleeding on probing (BOP) Bleeding on probing will be assessed at 1 year, 3 years, 5 years after final restoration Up to 5 years after final restoration
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