Skip to main content
MedPathMedPath Home
Clinical Trials/CTRI/2024/07/070005
CTRI/2024/07/070005
Not yet recruiting
Phase 2

A comparative 6 months evaluation of clinicaland radiographic outcome of necrotic singlerooted teeth obturated using two different bioceramic sealers : A CBCT-based randomizedclinical study - NI

Dr Riddhi Vasa0 sites0 target enrollmentTBD
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
ConditionsHealth Condition 1: K041- Necrosis of pulp

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: K041- Necrosis of pulp
Sponsor
Dr Riddhi Vasa
Status
Not yet recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Dr Riddhi Vasa

Eligibility Criteria

Inclusion Criteria

  • •Inclusion criteria
  • •1\.Systemically healthy patients (Category: American Society of Anesthesiologists Class 2 or less than 2\) 25 between 18 – 65 years of age.
  • •2\.Maxillary or mandibular single rooted teeth diagnosed with Pulpal necrosis with symptomatic or asymptomatic apical periodontitis with lesions that show periapical radiolucency with (CBCTPAI) Score 323 will be included in the study.
  • •3\.Re\-treatment cases with periapical lesions with CBCTPAI Score 3 will be included in the study.
  • •4\.A written informed consent will be taken from all the patients and only those patients ready to sign the consent form will be included in the study.

Exclusion Criteria

  • •Exclusion criteria
  • •1\.Pregnant and lactating women will be excluded.
  • •2 Patients having teeth with poor prognosis, open apices, internal/external resorption, fractured Roots or visibly cracked tooth, grade 3 mobility, severe periodontal bone loss will be excluded from the study
  • •3\.Patients having teeth with complex root canal morphology such as Calcified canals, extreme curvatures or anomalies will be excluded from the study.

Outcomes

Primary Outcomes

Not specified

Similar Trials

Completed
Not Applicable
The effect of duration of treatment with valganciclovir in children with renal transplantatioCondition 1: renal failure. Condition 2: CMV infection.Acute renal failureOther and unspecified infectious diseases
IRCT2015021321062N1Iran University of Medical Sciences86
Unknown
Phase 4
Comparison One vs Six Months of Dual Antiplatelet Therapy After Implanted Firehawk TM Stent in High Bleeding Risk Patients With Coronary Artery DiseaseCoronary DiseaseDrug Eluting StentPercutaneous Coronary InterventionDual Antiplatelet Therapy
NCT03287167Shanghai MicroPort Medical (Group) Co., Ltd.1,720
Active, not recruiting
Phase 1
Therapeutic efficacy comparison of a six-month treatment by itraconazole and nebulised Ambisome® versus treatment by itraconazole alone in non- or mildly- immunocompromised patients with Chronic Pulmonary Aspergillosis: a prospective, randomized, single blind study, (single aspergilloma excluded).MedDRA version: 20.1 Level: LLT Classification code 10022881 Term: Invasive bronchopulmonary aspergillosis System Organ Class: 100000004862Therapeutic area: Body processes [G] - Circulatory and Respiratory Physiological Phenomena [G09]
EUCTR2018-000972-14-FRCHU DE POITIERS224
Not yet recruiting
Not Applicable
Comparative study of 2 root coverage procedures of teethHealth Condition 1: null- Patients with bilateral maxillary gingival recessions â?¥2mm classified as Millers class 1 in the esthetic zone of the oral cavity with gingival biotype â?¥1mm without any systemic complications
CTRI/2017/12/010795Manipal college of Dental Sciences Mangalore
Not yet recruiting
Phase 2
Comparing The Clinical Performance Of Activaâ?¢ Bioactive Composite With Microhybrid Composite In Non Carious Cervical Lesions
CTRI/2020/05/025235DR PRATHIMA B J