- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02290158
Effects of a Finishing Protocol Implementation in Orthodontic Patients
7. december 2015 opdateret af: Alvaro Carvajal, Universidad de Antioquia
Effects of a Finishing Protocol Implementation on the American Board of Orthodontics - Objective Grading System Score in Patients of Orthodontic Postgraduate Program: A Quasiexperimental Clinical Trial
This study evaluates the effects of a finishing protocol in orthodontic outcomes using ABO-OGS scores.
Patients who finish orthodontic treatment and fulfill the inclusion and exclusion criteria receive a treatment using a finishing protocol and their scores are compare with 40 patients who don't receive a finishing protocol
Studieoversigt
Detaljeret beskrivelse
The phase of finishing is the most demanding and detailed of all phases of the orthodontic treatment.
American Board of Orthodontics- Objective Grading system is a detailed and objective method that evaluates the quality of the final outcome of orthodontic treatment.
In order to evaluate and compare the effects of a protocol implementation on the ABO-OGS scores, standardize cast models and Pan X-Ray from by convenience patients of Orthodontic Postgraduate Program of University of Antioquia who finish orthodontic treatment and receive the protocol are digitized, eight variables are evaluate and ABO-OGS score is calculate.
A comparison with 40 no-protocol ABO-OGS scores by convenience-selected patients is done.
The protocol includes an educate residents program about finishing problems , an standardized clinical and X-ray assessment , brackets reposition and frequent clinical evaluation.
The percentage of the protocol implementation is calculate in every patient and reliability test is make .
The descriptive analysis and the ABO-OGS score comparison is done by Pearson or Spearman correlation.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
34
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Antioquia
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Medellin, Antioquia, Colombia
- Uniersidad de Antioquia
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-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Patients who finish orthodontic treatment by orthodontic criteria
- Receive finishing protocol
- Accept and sign inform consent
- Records ( Panoramic Xray and cast models) taken immediately or 7 days after orthodontic appliances are remove
Exclusion Criteria:
- Patients who don't accept being at the study
- Bad quality records
- Prosthodontic, periodontic and surgical needs treatment after orthodontic treatment
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Enkelt gruppeopgave
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: Orthodontic finishing
Patients receiving a complete orthodontic finishing protocol according to the ABO-OGS
|
Students education, cast models and Panoramic X-ray assessment, brackets reposition and frequent clinical evaluation.
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|
Ingen indgriben: No orthodontic finishing
Patients receiving orthodontic treatment without the finishing protocol according to the ABO-OGS
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
ABO-OGS Total Score
Tidsramme: Until 7 days after orthodontic appliances are removed
|
Sum of 8 variables scores ( alignment, marginal ridge height, buccolingual inclination, overjet, interproximal contact, occlusal contacts, occlusal relationships, and root angulation ) 1: difference less than 1 mm, 2: difference between 1 and 2 mm, 3: difference bigger than 2 mm .
Total score less than 20: Excellent , Total score between 20-30: Acceptable and Total Score: > 30 No acceptable
|
Until 7 days after orthodontic appliances are removed
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Line Smile
Tidsramme: Until 7 days after orthodontic appliances are removed
|
Gingival exposure in smiling photo: High: More than 2 mm of gingival exposure, Media: between 2 and O mm of gingival exposure , Low: Less than clinical crown
|
Until 7 days after orthodontic appliances are removed
|
|
Arch Smile
Tidsramme: Until 7 days after orthodontic appliances are re
|
Relationship between incisor borders and upper lower lip border in an smiling photo
|
Until 7 days after orthodontic appliances are re
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. juni 2013
Primær færdiggørelse (Faktiske)
1. juni 2015
Studieafslutning (Faktiske)
1. september 2015
Datoer for studieregistrering
Først indsendt
26. oktober 2014
Først indsendt, der opfyldte QC-kriterier
8. november 2014
Først opslået (Skøn)
13. november 2014
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
8. december 2015
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
7. december 2015
Sidst verificeret
1. november 2014
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- BACAZA1
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .