Effect of Cavity Disinfectants on Post Operative Pain & Success of Partial Caries Removal
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Selective caries removal, Selective caries removal with NaOCl, Selective caries removal with CHX.
- Who it may be relevant to
- Registry conditions: Pulp Disease, Dental. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- India
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
The Effect of Sodium Hypochlorite and Chlorhexidine as Cavity Disinfectants on the Post Operative Pain and Success of Partial Caries Removal in Deep Carious Lesion With Moderate Pulpitis in Permanent Teeth: A Randomized Controlled Trial
Overview
To investigate The Effect of Sodium hypochlorite and Chlorhexidine as cavity Disinfectants on the post operative pain and Success of Partial Caries Removal in deep carious lesion with moderate pulpitis in permanent teeth
Detailed description
Study Design: Intervention Research Question : To investigate whether the use of 2% chlorhexidine and 5.25% sodium hypochlorite can improve the clinical and radiographic outcome after partial caries removal in deep carious lesion P (Population) - Mature Permanent Mandibular molars with deep carious lesion involving inner two third of dentine I (Intervention) - - Partial caries removal using 2% chlorhexidine/5.25% sodium hypochlorite as cavity disinfectant..
C (Comparison) - Partial caries removal using saline as cavity disinfectant. O (Outcome) - Assessment of clinical and radiographic success at 12 months follow up.
-To assess incidence and reduction in pain post operatively at every 24 hours till 1 week.
Interventions
- Procedure Selective caries removal
Selective caries removal followed by cavity disinfection with NaOCl \& CHX in each test group \& no cavity disinfection in control group. - Procedure Selective caries removal with NaOCl
elective caries removal followed by cavity disinfection with NaOCl - Procedure Selective caries removal with CHX
elective caries removal followed by cavity disinfection with CHX
Primary outcome measures
- Clinical success criteria [Time frame: 12 months]
- Radiographic success criteria [Time frame: 12mnths]
Secondary outcome measures (1)
- Pain assesment [Time frame: 7 days]
Eligibility criteria
Inclusion criteria
- The patient should be ≥18 years of age.
- Restorable mature permanent 1st and 2nd Mandibular molars with extremely deep caries (≥2/3 dentine involvement)
- Tooth should give positive response to pulp sensibility testing.
- Clinical diagnosis of moderate pulpitis.
- Radiographic finding of periapical index (PAI) score ≤2.
- Healthy periodontium (probing pocket depth ≤3 mm and mobility within normal limit)
Exclusion criteria
Presence of vertical root fracture Presence of root perforations ASA-3 or ASA-4 according to the classification of the American Society of Anesthesiologists) Presence of root resorption Combined endodontic-periodontic lesions. Pregnancy
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Triple blind
- Primary purpose
- Treatment
Study locations
India · 1 center
- Pgids Rohtak — Haryāna
Identifiers
NCT: NCT06836882 · shweta mittal