UnknownNot Applicable

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

Thailand60 participantsStarted 2022-06-01

Plain-language 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.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

soft tissue alteration

Timeframe: T0 baseline before implant placement,T1 1month follow up, 4month follow up, 6month follow up, 12month follow up

hard tissue alteration

Timeframe: T0 baseline before implant placement, 6month follow up, 12month follow up

volumetric alteration

Timeframe: T0 baseline before implant placement,T1 1month follow up, 4month follow up, 6month follow up, 12month follow up

Trial details

NCT IDNCT06125418

SponsorChiang Mai University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-12-20

View on ClinicalTrials.gov More Peri-implant Tissue Response With Use of Customized Healing Abutments trials

Plain-language summary

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

soft tissue alteration

Timeframe: T0 baseline before implant placement,T1 1month follow up, 4month follow up, 6month follow up, 12month follow up

hard tissue alteration

Timeframe: T0 baseline before implant placement, 6month follow up, 12month follow up

volumetric alteration

Timeframe: T0 baseline before implant placement,T1 1month follow up, 4month follow up, 6month follow up, 12month follow up