Effect of Customized Healing Abutments on Peri-implant Soft Tissue and Bone

Sponsor
Chiang Mai University (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT06125418
Collaborator
(none)
60
1
2
42.6
1.4

Study Details

Study Description

Brief Summary

The goal of this clinical trial is to evaluate effect of customized healing abutment in patients who need single implant reconstruction. The main question it aims to answer is:

• effect of customized healing abutment on peri-implant soft and hard tissue Participants will received customized healing abutments before final prostheses delivery.

Condition or Disease Intervention/Treatment Phase
  • Procedure: customized healing abutment
  • Procedure: standard healing abutment
N/A

Detailed Description

Patients who need single implant restoration will be received one- stage implant placement with utilization of customized healing abutment. Data collection about change in hard and soft tissue will be collected digitally at several times points. Patients will received single crown on implant as final prosthesis. Change in peri-implant tissue will be analyzed with digital softwares.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
patients in each group will received different types of customized healing abutmentpatients in each group will received different types of customized healing abutment
Masking:
Double (Participant, Care Provider)
Primary Purpose:
Treatment
Official Title:
Effect of Customized Healing Abutments on Peri-implant Soft Tissue and Bone
Actual Study Start Date :
Jun 1, 2022
Anticipated Primary Completion Date :
Dec 20, 2023
Anticipated Study Completion Date :
Dec 20, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Customized group

patients who received customized healing abutments following implant placement. customized healing abutments will be fabricated with different macrogeometry and different emergence angle

Procedure: customized healing abutment
patients will undergoes one-stage implant placement with customized healing abutments with different macrogeometry and emergence angle made prior to the surgery and will be inserted without sutures, after osseointegration completed patients will received single crown on implant.

Experimental: Standard group

patients who received standard titanium healing abutments following implant placement

Procedure: standard healing abutment
patients will undergoes one-stage implant placement with standard titanium healing abutment made prior to the surgery and will be inserted without sutures, after osseointegration completed patients will received single crown on implant.

Outcome Measures

Primary Outcome Measures

  1. soft tissue alteration [T0 baseline before implant placement,T1 1month follow up, 4month follow up, 6month follow up, 12month follow up]

    peri-implant soft tissue change compared to baseline including vertical and horizontal soft tissue alteration by superimposing intraoral scan at different time points

  2. hard tissue alteration [T0 baseline before implant placement, 6month follow up, 12month follow up]

    peri-implant marginal bone change compared to baseline at different time points by periapical radiograph

  3. volumetric alteration [T0 baseline before implant placement,T1 1month follow up, 4month follow up, 6month follow up, 12month follow up]

    peri-implant volumetric change at different time points compared to baseline with superimposing intraoral scan

Secondary Outcome Measures

  1. pain numerical rating scale [at prosthesis delivery, 2 hours and 24 hours after prosthesis delivery]

    pain assessment at time of final prosthesis delivery with scale from 0 to 10

  2. pink esthetic score [T0 baseline before implant placement, 6 month follow up]

    pink esthetic score change compared to before implant treatment

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • ≥18 years of age;

  • patients who needed a single implant placing therapy in maxillary or mandibular arch except in third molar regions

  • sufficient mesial distal and interocclusal space for placement of the implant and definitive restoration;

  • had sufficient apical bone to place an implant with minimum primary stability of 30 Ncm.

Exclusion Criteria:
  • medical and general contraindications for the surgical procedure;

  • heavy smokers (>10 cigarettes/day);

  • an active infection at the implant site.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Prosthodontics, Faculty of Dentistry, Chiang Mai University Chiang Mai Thailand 50300

Sponsors and Collaborators

  • Chiang Mai University

Investigators

  • Principal Investigator: Pimduen Rungsiyakull, AssocProfDr, Chiang Mai University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Pimduen Rungsiyakull, Associate Professor, Chiang Mai University
ClinicalTrials.gov Identifier:
NCT06125418
Other Study ID Numbers:
  • 43/2022
First Posted:
Nov 9, 2023
Last Update Posted:
Nov 9, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Pimduen Rungsiyakull, Associate Professor, Chiang Mai University

Study Results

No Results Posted as of Nov 9, 2023