Healing Outcomes of Peri-implant Soft Tissues With Different Healing Abutments

Conditions

• Implant

Eligibility Criteria

Sex

ALL

Age

18 Years - N/A

Healthy Volunteers

Not accepted

Interventions

• Healing Abutment- customized — DEVICE
  A customized healing abutment will be used on subjects in this study as part of their implant healing process.
• Healing Abutment- pre fabricated — DEVICE
  A pre-fabricated (pre- made) healing abutment will be used on subjects in this study as part of their implant healing process.

Study Details

The purpose of this study is to compare how well our research participants heal with two different kind of healing abutments used. One is pre-fabricated, meaning it is made to fit anyone, and the other is customized to fit the subject specifically. Much of what will occur is 'standard of care' meaning it is part of a subject's typical dental treatment and the research team wants to just look at the data for this research study, as well.

Key Dates

Start date

Jan 22, 2026

Status verified

Jan 2026

Primary completion

Jan 1, 2027

Completion

Jan 1, 2028

Study Design

Enrollment

48 participants (estimated)

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Arms

• Active Comparator: Control: Pre Fabricated Healing Abutment
  Subjects that are randomized into the control group will have a pre-fabricated healing abutment used.
• Experimental: Investigational: Customized Healing Abutment
  Subjects that are randomized into the control group will have a customized healing abutment used.

Primary Outcome Measure

Soft tissue healing progress [ Time Frame: 3 months ]

Central Contacts

• Lorenzo Mordini
  857-299-4168
  [email protected]
• Ann-Marie Jacobson
  [email protected]

Locations (1)

Find similar trials in Boston, MA

Related Studies

• Carotid Implants for PreveNtion of STrokE ReCurrEnce From Large Vessel Occlusion in Atrial Fibrillation Patients Treated With Oral Anticoagulation
  Recruiting · Javelin Medical · Rockford, Illinois