- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07906236
Esthetic Impact of Different Minimally Invasive Approaches on Hypomineralized Permanent Anterior Teeth
Esthetic Impact of Different Minimally Invasive Approaches on Hypomineralized Permanent Anterior Teeth: A Randomized Clinical Trial
The aim of the study is to determine the effectiveness of minimally invasive treatments in reducing the visible enamel opacities on permanent anterior teeth in children aged from seven to twelve years with hypomineralized lesions.
A secondary purpose is to evaluate patient satisfaction and the psychosocial impact of the treatment on the esthetic perception of the treated children.
The results of all the research papers about treating enamel discoloration caused by hypomineralization with the ICON system can be accepted as satisfactory. However, not all cases achieved the full aesthetic aim.
Microabrasion is an acid abrasive removal and not the dissolution of enamel stain. It is as a treatment modality for enamel opacities like brown, orange, or yellow enamel spots; and fluorotic white streaks. Esthetic results could be reached when microabrasion followed by a remineralizing agent such as C PP-ACFP.
Null hypothesis, there is no difference between microabrasion followed by a remineralizing agent and resin infiltration treatment regarding clinical effectiveness & patient satisfaction.
Studienübersicht
Status
Bedingungen
Detaillierte Beschreibung
Outcomes:
Primary outcome Color enhancement using Clinical photographs (Bhandari, et al., 2019). Secondary outcomes
- Patient satisfaction will be evaluated using Numerical scale (NS), (Figure 1). The participant marked the number that represented their self-assessed satisfaction (Rocha et al., 2020) as shown in Appenxix II.
- Psychosocial impact of the treatment on the esthetic perception of the treated children will be evaluated using The Psychosocial Impact of Dental Aesthetics Questionnaire (PIDAQ) (Klages et al., 2006). Appendix III.
- Reducing teeth hypersensitivity will be evaluated using The Schiff Cold Air Sensitivity Scale (SCASS) (Schiff et al., 1994).
- Adverse and undesirable side effects experienced by the respondents: a) pain in teeth and gums will be evaluated using The Wong-Baker FACES® Pain Rating Scale (Wong et al., 1988). Appendix IV.
- b) bitter taste will be evaluated by asking the child right after treatment. (Athayde et al., 2022).
- Follow up:
Follow up after 1 day for adverse and undesirable side effects, 1week & 6 months.
Randomization:
The participants will be randomly assigned to one of the three experimental groups the interventions and control groups using simple randomization with a 1:1 allocation ratio.
Masking/blinding:
Neither the operator nor the patients could be blinded due to the nature of the study but the outcome assessor and statistician will be blinded.
Studientyp
Einschreibung (Geschätzt)
Phase
- Unzutreffend
Kontakte und Standorte
Studienkontakt
- Name: Shaimaa AM Awad, Mcs
- Telefonnummer: 01027557531
- E-Mail: shaimaa.awad@dentistry.cu.edu.eg
Studieren Sie die Kontaktsicherung
- Name: Aliaa AM Awad
- Telefonnummer: 01062811856
- E-Mail: shaimaa.awad@dentistry.cu.edu.eg
Studienorte
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Cairo, Ägypten
- Faculty of Dentistry, Cairo University
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Kontakt:
- Shaimaa Awad, Mcs
- Telefonnummer: 01027557531
- E-Mail: shaimaa.awad@dentistry.cu.edu.eg
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
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▪ Participants free from any systemic disease aged from 7 years to 12 years
- Anterior permanent teeth with Degree 1(mild) hypomineralization (according to the Wetzel and Reckel scale) (as shown in Appenxix I).
- Enamel opacities, (White, creamy or yellow to brownish colour), without enamel breakdown
- Caries-free teeth.
- Sensitivity to external stimuli e.g., air/water but not brushing.
Exclusion Criteria:
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▪ Dental caries and filling,
- Loss of the enamel or dentin structure,
- Clinical symptoms of irreversible pulpitis such as spontaneous pain or persisting pain,
- Previous use of bleaching agent.
- Dental anomaly on anterior teeth,
- Periodontal diseases,
- Undergoing orthodontic treatment,
- Cognitive and behavioral conditions.
- Patients with milk protein or hydroxybenzoates allergies.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Aktiver Komparator: Control group ICON® resin infiltration
Resin infiltration treatment (Icon®) for Hypomineralized anterior permanent teeth in children |
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Experimental: Intervention group 1
Opalustre® Enamel Microabrasion Slurry |
NOTE: For hypo-mineralization greater than 0.1-0.3mm use a fine-grit water-cooled tapered diamond bur, lightly sweep over the stained area for 5-10 seconds prior to applying Opalustre.
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Experimental: Intervention group 2
Antivet® enamel micro-abrasion |
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Color enhancement measured by Clinical photographs
Zeitfenster: 6 months
|
Clinical photographs will be taken with a digital camera macro lens, and flash. With the patient and digital camera at the same vertical plane and dental clinic illuminated evenly. The photographs will be taken in baseline, during the application time of the test or control. For standardizing the photographic conditions, the camera will be placed at the equidistance from the tooth. To prevent the change of refractive index by moisture, 30 s of drying of the lesion will be done. |
6 months
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Patient satisfaction measured by Visual analogue scale
Zeitfenster: 6 months
|
The patient is asked to draw a line perpendicular to the VAS at their perceived pain-intensity level, no discomfort (score 0), mild discomfort (score 1-3), moderate (score 4-6) and very severe (7-9) or worst discomfort (score 10). |
6 months
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Reducing teeth hypersensitivity measured by The Schiff Cold Air Sensitivity Scale (SCASS)
Zeitfenster: 6 months
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It is a behavioral scale because it is based on observed behavior in response to a stimulus beyond a certain threshold. The dentist (or another assessor present) rates the response of the patient to the stimulus as 0 for no response to air stimulus,
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6 months
|
Mitarbeiter und Ermittler
Sponsor
Ermittler
- Hauptermittler: Shaimaa AM Awad, Mcs, Cairo Uviversity
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 261711198415920202321948291954
Plan für individuelle Teilnehmerdaten (IPD)
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