CompletedNot Applicable

Outcome Following Use of NaOCl and Chlorhexidine as Wound Lavage Agents

India142 participantsStarted 2022-07-01

Plain-language summary

The goal of this clinical trial is to to compare effect of wound lavage agents NaOCl and Chlorhexidine on the outcome of partial pulpotomy in mature permanent posterior teeth with signs and symptoms indicative of irreversible pulpitis in. The main question it aims to answer are: Does wound lavage using chlorhexidine have equal effect as NaOCl on the outcome of partial pulpotomy in mature permanent mandibular posterior teeth with clinical signs of irreversible pulpitis? Participants will of age group 18 to 45 years will be included and divided into two groups: Pulp wound lavage in partial pulpotomy using 3% NaOCl as control and using 2% Chlorhexidine as experiment

Who can participate

Age range18 Years – 45 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Mature permanent mandibular posterior teeth with extreme deep caries and clinical diagnosis of symptomatic irreversible pulpitis * Patients having normal periapical status with periapical index (PAI) score ≤ 2 and periodontally healthy teeth * Patients having physical status of class 1 or 2 according to ASA classification * Pulpal bleeding can be controlled within 10 minutes Exclusion Criteria: * Necrotic pulp upon exposure * Presence of sinus tract or soft tissue swelling Pregnant patients Radiographic signs of internal or external root resorption

What they're measuring

Clinical Success and Radiographic Success

Timeframe: Base line to 12 months

Trial details

NCT IDNCT06240130

SponsorPostgraduate Institute of Dental Sciences Rohtak

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-03-01

View on ClinicalTrials.gov More Irreversible Pulpitis trials