- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07825415
"The Relationship Between Pulpal Inflammatory Marker Levels in Moderate and Severe Pulpitis and Outcome of Full Pulpotomy in Mandibular Molars With Extremely Deep Caries: A Prospective Cohort Study."
Study Title: - The Relationship between pulpal inflammatory marker levels in moderate and severe pulpitis and outcome of full pulpotomy in mandibular molars with extremely deep caries: A prospective cohort study." RATIONALE: - Dental caries-induced pulpal inflammation represents a dynamic biological process in which the intensity of the host immune response increases with lesion depth. Extremely deep caries can be present clinically as moderate or severe pulpitis where the pulp inflammation is extensive and confine in the crown or possibly extend itself into the root canals respectively. Clinical diagnostic methods used to identify this stage are largely subjective and often fail to reflect the true biological status of the pulp, leading to inconsistent treatment outcomes.
Aim & Objectives- To assess and compare the levels of IL-1Beta and IL-6 in extremely deep caries in moderate and severe pulpitis and to correlate these levels with treatment outcomes of full pulpotomy. Setting: - Study will be conducted in Post Graduate Institute of Dental Sciences, Rohtak in department of Conservative Dentistry & Endodontics. Study Design: - Prospective cohort study Time Frame: - 12-18 months Participants: -Inclusion criteria:- o Medically healthy patients (ASA 1). o Age 18-40 years o Patients with extremely deep caries in permanent mandibular molars. o Extremely deep caries, that is penetrating the entire thickness of the dentine without a radiopaque zone separating the lesion from the pulp o PAI score less then or equal to 2 o Pulpal diagnosis via clinical and radiographic examination as well as thermal, electric pulp testing, categorized as moderate pulpitis (Heightened and prolonged reaction to cold, which can last for minutes Possible percussion sensitive Stimulated or spontaneous lingering pain that can be suppressed with analgesics. No sleep disturbance) or severe pulpitis (Severe spontaneous pain Clear lingering pain reaction to cold and warms stimuli Sleeping disturbance and lingering pain Possible sensitive to percussion Extremely deep caries mostly). Exclusion criteria • Primary teeth • Traumatic or mechanical exposure • No pulp exposure after caries excavation. • Haemostasias not achieved within 10 minutes. • Presence of periapical lesion or evidence of internal or external resorption, calcified canals, as assessed by radiographic examination. • Patients with periodontal disease, swelling and sinus tract. • Immunocompromised or pregnant patients, patients with any systemic disease, and a positive history of antibiotic and analgesic use within week before the treatment. Sample size: -86 (43per group) Outcome variables: Primary outcome: Levels of IL-1beta and IL-6 in extremely deep caries in moderate and severe pulpitis Secondary outcome: To assess the correlation between the marker levels and clinical and radiographic success of full pulpotomy at 6 and 12 months interval. Statistical method: - The normality of the data will be checked by Shapiro-Wilks test in SPSS software. If the data will be non-normal, then non-parametric tests will be applied. Intergroup and intra group comparison will be done according to distribution of data. Categorical data will be analysed using chi-square test. Regression analysis will be done to observe any association between dependent and independent variable. The Spearman rank correlation test will be used to measure the strength of association between concentration of IL-6 ,IL-1Beta in pulpal blood samples.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Dr. Akankshya Pattnaik, PG student
- Numéro de téléphone: 8658292111
- E-mail: akankshyapattnaik44@gmail.com
Sauvegarde des contacts de l'étude
- Nom: Dr. Jigyasa Duhan, MDS
- Numéro de téléphone: 98962 70449
Lieux d'étude
-
-
Haryana
-
Rohtak, Haryana, Inde, 124001
- Recrutement
- PGIDS, Rohtak
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
Accepte les volontaires sains
La description
Inclusion Criteria:
o Medically healthy patients (ASA 1).
- Age 18-40 years
- Patients with extremely deep caries in permanent mandibular molars.
- Extremely deep caries, that is penetrating the entire thickness of the dentine without a radiopaque zone separating the lesion from the pulp
- PAI score less then or equal to 2
- Pulpal diagnosis via clinical and radiographic examination as well as thermal, electric pulp testing, categorized as moderate pulpitis (Heightened and prolonged reaction to cold, which can last for minutes Possible percussion sensitive Stimulated or spontaneous lingering pain that can be suppressed with analgesics. No sleep disturbance) or severe pulpitis (Severe spontaneous pain Clear lingering pain reaction to cold and warms stimuli Sleeping disturbance and lingering pain Possible sensitive to percussion Extremely deep caries mostly).
Exclusion Criteria:
• Primary teeth
- Traumatic or mechanical exposure
- No pulp exposure after caries excavation.
- Haemostasias not achieved within 10 minutes.
- Presence of periapical lesion or evidence of internal or external resorption, calcified canals, as assessed by radiographic examination.
- Patients with periodontal disease, swelling and sinus tract.
- Immunocompromised or pregnant patients, patients with any systemic disease, and a positive history of antibiotic and analgesic use within week before the treatment.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Non randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: extremely deep caries in moderate pulpitis
|
After removal of Caries in accordance with the standard protocol complete de- roofing of the pulp chamber will be carried out and pulp tissue will be removed to the root canal orifices.
A standard volume of 100 μL of pulpal blood sample will be collected using a single channel micropipette.
Haemostasis will be achieved using 3% sodium hypochlorite.
MTA will be used as a pulp capping material followed by restoration with composite.
The quantification of molecular markers will be done using ELISA.
|
|
Expérimental: extremely deep caries in severe pulpitis
|
After removal of Caries in accordance with the standard protocol complete de- roofing of the pulp chamber will be carried out and pulp tissue will be removed to the root canal orifices.
A standard volume of 100 μL of pulpal blood sample will be collected using a single channel micropipette.
Haemostasis will be achieved using 3% sodium hypochlorite.
MTA will be used as a pulp capping material followed by restoration with composite.
The quantification of molecular markers will be done using ELISA.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Levels of IL-1beta and IL-6 in extremely deep caries in moderate and severe pulpitis
Délai: 12 months
|
12 months
|
Collaborateurs et enquêteurs
Les enquêteurs
- Chercheur principal: Dr. Akankshya Pattnaik, Postgraduate Institute of Dental sciences, Rohtak 124001
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Autres numéros d'identification d'étude
- Akankshya Pattnaik
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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