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Comparative Evaluation of the Post Operative Sensitivity of Cention-N(Commercially Available Restorative Material) Using Conventional and Polymer Bur- In-vivo Study
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Dental caries is a multifactorial disease which is very much prevalent in India occurring especially in high economic group and some in middle and lower economic groups of world population.The most common instruments used for excavation of dental caries are the use of diamond and carbide burs.There is effective removal of the carious tooth structure through these burs which leads to excess removal of tooth structure and weakening the teeth.
Timely advancement in dentistry and the quest for the development of ideal esthetic materials to replace lost dental tissue has led to use of Cention-N(commercially available restorative material) to restore posterior teeth. Cention N(commerically available restorative material) is a recently introduced tooth-coloured, basic filling material for bulk placement in retentive preparations with or without the application of an adhesive. It is an alkise restorative which is a new category of filling material, like compomer(commercially available restorative material) or ormocer(commercially available restorative material) and is essentially a subgroup of the composite resin. Cention-N(commercially available restorative material)offers a cost-effective substitute for amalgam and also fulfills the need of an esthetic bulk fill material in the posterior region. Patients have described post-operative sensitivity as a moderate pain, of short duration, that appears spontaneously when chewing, with hot and cold foods and on rare occasions with sweet and acid foods, and it disappears when the stimulus is removed. It is characterized by an acute pain that can last for days or weeks and disappears when the stimulus is removed.It results from the interaction between the restorative technique, the clinical condition of the tooth to be treated (health of the pulp and remaining hard dental tissue) and the restorative material. Therefore, there is a permanent and unpredictable possibility of sensitivity occurring. In addition, there are other factors related to the cause of post- operative sensitivity, such as the individual profile of each patient, the shape and extension of the cavity preparation and protection of the dentin-pulp complex. Hence the novelty of this study is to evaluate of the post operative sensitivity of Cention-n (commerically available restorative material)using conventional and polymer bur.
Studietype
Inschrijving (Verwacht)
Fase
- Niet toepasbaar
Contacten en locaties
Studiecontact
- Naam: Soumya S Shetty, MDS
- Telefoonnummer: 8888200888
- E-mail: drsoumyasshetty@gmail.com
Studie Locaties
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Maharashtra
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Pune, Maharashtra, Indië, 411018
- Werving
- Dr D.Y. Patil Dental College and Hospital, Pimpri
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Contact:
- Soumya S Shetty, MDS
- Telefoonnummer: 888820088
- E-mail: drsoumyasshetty@gmail.com
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Contact:
- Riya A Parwani, BDS
- Telefoonnummer: 9922929705
- E-mail: riyaparwani2307@gmail.com
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Patients aged between 18 and 55 years having class 1 occlusal caries(1.2 according to G. J. Mount classification) on both sides of arch. In order to standardise the cavity preparation depth(approximately 1.5 to 2mm from the roof of the pulp chamber), the distance from occlusal surface to roof of pulp chamber will be used for measuring with the radiograph.
- Roots with closed apex.
- Systematically healthy patients.
- Patients with no other symptomatic tooth involved
Exclusion Criteria:
- Teeth with the presence of any pathologic pulpal disease with or without pain.
- Teeth with previous restorations, any defective restoration adjacent to or opposing the affected tooth.
- Teeth with surface loss due to attrition, erosion, abrasion, or abfraction.
- Patients with poor oral hygiene, severe, or chronic periodontitis.
- Patient on medication which may hinder the response to sensitivity.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verdrievoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
---|---|
Actieve vergelijker: Analysis of post-operative sensitivity after caries removal using conventional steel bur
Caries will be excavated using a carbide on one side of the arch and restoration will be done with Cention-N(commercially available restorative material) as per manufacturer's instructions.Thermal stimulation (refrigerant spray Endo-Ice) will be used to evaluate the type of sensitivity.
The pain intensity will be recorded with the Visual Analog Scale.
|
Patients aged between 18 and 55 years having class 1 occlusal caries(1.2
according to G. J. Mount classification) on both sides of arch.
In order to standardise the cavity preparation depth(approximately 1.5 to 2mm from the roof of the pulp chamber), the distance from occlusal surface to roof of pulp chamber will be used for measuring with the radiograph.
This will be followed by caries removal with convention steel bur followed by restoration with Cention-n and checking of postoperative sensitivity using Visual Analog Scale.The Visual Analog Scale consists of a 100-mm line divided into equal intervals of 10 mm, where 0 represents "absence of pain" and 100 "severe pain."
The results of Visual Analog Scale will be classified as mild (0-30 mm), moderate (40-70 mm), or severe pain (> 70 mm).
|
Experimenteel: Analysis of post-operative sensitivity after caries removal using polymer bur
Caries will be excavated using a polymer on one side of the arch and restoration will be done with Cention-N(commercially available restorative material) as per manufacturer's instructions.Thermal stimulation (refrigerant spray Endo-Ice) will be used to evaluate the type of sensitivity.
The pain intensity will be recorded with the Visual Analog Scale.
|
Patients aged between 18 and 55 years having class 1 occlusal caries(1.2
according to G. J. Mount classification) on both sides of arch.
In order to standardise the cavity preparation depth(approximately 1.5 to 2mm from the roof of the pulp chamber), the distance from occlusal surface to roof of pulp chamber will be used for measuring with the radiograph.
This will be followed by caries removal with polymer bur followed by restoration with Cention-n and checking of postoperative sensitivity using Visual Analog scale.The Visual Analog Scale consists of a 100-mm line divided into equal intervals of 10 mm, where 0 represents "absence of pain" and 100 "severe pain."
The results of Visual Analog Scale will be classified as mild (0-30 mm), moderate (40-70 mm), or severe pain (> 70 mm).
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
---|---|---|
Post-operative sensitivity checked using Visual Analog Scale by thermal stimulus.
Tijdsspanne: Post operative sensitivity will be checked after 24 hours.
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Thermal stimulation (refrigerant spray Endo-Ice) will be used to evaluate the type of sensitivity.
The pain intensity will be recorded with the visual analog scale (VAS).
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Post operative sensitivity will be checked after 24 hours.
|
Post-operative sensitivity checked using Visual Analog Scale by thermal stimulus.
Tijdsspanne: Post operative sensitivity will be checked after 15 days.
|
Thermal stimulation (refrigerant spray Endo-Ice) will be used to evaluate the type of sensitivity.
The pain intensity will be recorded with the visual analog scale (VAS).
|
Post operative sensitivity will be checked after 15 days.
|
Post-operative sensitivity checked using Visual Analog Scale by thermal stimulus.
Tijdsspanne: Post operative sensitivity will be checked after 30 days.
|
Thermal stimulation (refrigerant spray Endo-Ice) will be used to evaluate the type of sensitivity.
The pain intensity will be recorded with the Visual Analog Scale.
|
Post operative sensitivity will be checked after 30 days.
|
Medewerkers en onderzoekers
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Verwacht)
Studie voltooiing (Verwacht)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- DYPDCH/IEC/123/99/19
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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