Clinical Trial of Modified Endocrown and Personalized Post-core and Crown for Large-area Tooth Defects After Root Canal Treatment
Recruiting
N/A
Interventional Study
Root Canal Infection
Tooth Defect
Post and Core Technique
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 65
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 246 (estimated)
- Sponsor
- Nanfang Hospital, Southern Medical University · Other
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About This Trial
This study intends to adopt a multicenter, randomized controlled, single-blind, non-inferiority clinical trial design. 246 premolars that meet the inclusion criteria after complete root canal treatment will be selected from the clinical practice and randomly divided into two groups. One group will be restored with the modified endocrown, and the other group will be restored with personalized post …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 1: The affected tooth was a premolar that had undergone complete root canal treatment for two weeks. Both imaging and clinical examinations indicated no abnormal periapical reactions.
2: The oral hygiene condition is good. There is no periodontitis or combined periodontal a…
Contacts
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