Viewing Study NCT06573463



Ignite Creation Date: 2024-10-26 @ 3:38 PM
Last Modification Date: 2024-10-26 @ 3:38 PM
Study NCT ID: NCT06573463
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-08-16

Brief Title: Longevity of Prefabricated Band and Loop Versus Conventional Band and Loop Space Maintainers
Sponsor: None
Organization: None

Study Overview

Official Title: Longevity of Prefabricated Band and Loop Versus Conventional Band and Loop Space Maintainers in Children With Prematurely Lost First Primary Molars
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To assess the longevity of prefabricated versus conventional band and loop space maintainers in children with prematurely lost first primary molars

A Randomized Clinical Trial
Detailed Description: When considering gingival health and cement dissolution does the longevity of the prefabricated band and loop differ from the conventional band and loop constructed following the premature loss of the lower first primary molars

The concept of preserving space after premature tooth loss has been recognized for over a century Conventional appliances are used successfully as space maintainers but some disadvantages like the need for at least two visits to deliver the appliance due to laboratory work will definitely affect its role during the general anesthesia

The prefabricated space maintainer requires only one visit as it is fitted into the patients mouth at the clinic without needing the dental lab This provides a good impact on apprehensive children as it reduces the number of visits and chairside time Prefabricated space maintainers could be a new alternative to the conventional fixed space maintainers used in pediatric dentistry

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None