CompletedNot Applicable

Outcome Following Use of Different Concentrations of NaOCl as Wound Lavage and Hemostatic Agent in Partial Pulpotomy

India128 participantsStarted 2024-05-23

Plain-language summary

The aim of this randomised control trial is to compare the effect of different concentrations of NaOCl on outcome of partial pulpotomy in teeth with clinical signs indicative of irreversible pulpitis. The main question it aims to answer are: 1. clinical and radiographic outcome of partial pulpotomy following use of 5% and 3% NaOCl in mature permanent teeth with clinical signs indicative of irreversible pulpitis. 2. OHRQoL and pain experience after use of 5% and 3% NaOCl during partial pulpotomy in teeth with clinical signs indicative of irreversible pulpitis.

Who can participate

Age range15 Years – 40 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 molars.
✓. Teeth with clinical diagnosis of symptomatic irreversible pulpitis
✓. Patients having normal periapical status with periapical index (PAI) score ≤ 2
✓. Periodontally healthy teeth
✓. Patients having physical status of class 1 or 2 according to ASA classification
✓. Pulpal bleeding can be controlled within 6 minutes.
✓. Presence of extremely deep carious lesion on radiograph -

What they're measuring

Clinical success rate

Timeframe: baseline to 12 months

Radiographic success rate

Timeframe: Baseline to 12 months

Trial details

NCT IDNCT06433245

SponsorPostgraduate Institute of Dental Sciences Rohtak

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-12-23

View on ClinicalTrials.gov More Irreversible Pulpitis trials