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The effect of one-time customized abutment with three different configurations on human peri-implant crestal bone level, A Randomized Clinical Trial Study (1-3 years follow-up)

The effect of one-time customized abutment with three different configurations on human peri-implant crestal bone level, A Randomized Clinical Trial Study (1-3 years follow-up)

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240924002
Enrollment
40
Registered
2024-09-24
Start date
2022-05-15
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Human peri-implant crestal bone level Peri-implant crestal bone level One abutment one time concept

Interventions

Healing abutments (control group) were placed on the day of surgery following conventional standard protocol. The healing abutment will be remove after 3 months for conventional impression, restoratio
Healing abutment (control group),Straight customized abutment ,Concave customized abutment,Convex customized abutment

Sponsors

Esthetic Restorative and Implant Dentistry Department
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients with missing teeth in Posterior region with remaining adjacent teeth in between, needing single implant. This condition allows the surgical guides to be tooth-supported design. 2.No pathological mobility of adjacent teeth that supported surgical guide. 3.CBCT radiograph and clinical examination reveal sufficient bone volume to support the implants. (Buccal bone and lingual bone thickness at least 2mm.) 4.No limited mouth opening 5.Age 20 years and over that able to sign consent form. 6.Good general health at the time of selection (ASA class I or II). Adequate oral hygiene

Exclusion criteria

Exclusion criteria: 1.Dehiscence or lack of buccal bone plate 2.Irradiation in the head and neck area 3.Immunosuppressed or immunocompromised patients 4.Treated or under treatment with intravenous amino-bisphosphonates 5.Uncontrolled diabetes 6.Addiction to alcohol or drugs 7.Adjacent tooth between dental implant has pocket depth>5mm. Heavy smoking (>10 cigarettes daily) 8.Parafunction

Design outcomes

Primary

MeasureTime frame
Vertical bone loss 1,3,6 months, 1 year, and once a year after the 1 year recall mm

Secondary

MeasureTime frame
Horizontal bone loss 1,3,6 months, 1 year, and once a year after the 1 year recall mm

Countries

Thailand

Contacts

Public ContactAdison Jirasuwannakul

Chulalongkorn University

ad_jayz2@hotmail.com0646646469

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026