Comparing two treatments for moderate pulpitis in adult molars
COMPARATIVE EVALUATION OF DIRECT PULP CAPPING AND COMPLETE PULPOTOMY IN MATURE PERMANENT MANDIBULAR MOLARS WITH CLINICAL SIGNS INDICATIVE OF MODERATE PULPITIS: RANDOMIZED CLINICAL TRIAL
This study tests whether a direct pulp capping or a complete pulpotomy works better for adults with moderate pulpitis in their back teeth.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 92 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | All |
| Sponsor | Postgraduate Institute of Dental Sciences Rohtak Academic / other |
| Locations | 1 site (Rohtak, Haryana) |
| Trial ID | NCT06447753 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of direct pulp capping versus complete pulpotomy in treating mature permanent mandibular molars diagnosed with moderate pulpitis. The study aims to determine which intervention leads to better healing outcomes by addressing the inflamed pulp tissue while eliminating the source of infection. Participants will undergo either treatment based on specific eligibility criteria, including age and dental condition. The trial will assess clinical responses and healing over time to provide insights into the best management strategies for this dental condition.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older with restorable mature permanent mandibular molars exhibiting signs of moderate pulpitis.
Not a fit: Patients with immature roots, signs of pulpal necrosis, or significant medical histories that could complicate treatment may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve treatment outcomes for patients with moderate pulpitis, potentially preserving their teeth and reducing the need for more invasive procedures.
How similar studies have performed: Other studies have shown promising results with similar approaches in vital pulp therapy, suggesting that this trial is building on established concepts in dental treatment.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1\. The patient should be ≥18 years of age. 2. Restorable mature permanent 1 st and 2nd Mandibular molars with extremely deep caries (≥2/3 dentine involvement) 3. Tooth should give positive response to pulp sensibility testing. 4. Clinical diagnosis of moderate pulpitis. 5. Radiographic finding of periapical index (PAI) score ≤2. 6. Healthy periodontium (probing pocket depth ≤3 mm and mobility within normal limit). \- Exclusion Criteria: 1. Teeth with immature roots. 2. No pulp exposure after caries excavation. 3. Bleeding could not be controlled in 6 minutes. 4. Signs of pulpal necrosis, sinus tract, swelling, insufficient bleeding after pulp exposure. 5. History of analgesic intake in previous 1 week, or antibiotic intake in 1 month. 6. Internal/external resorption. 7. Contributory medical history (alcoholism, smokers, diabetic, hypertension, drug dependency, Heart or valve disease, hepatitis, herpes, immunodeficiency (HIV), infectious diseases, kidney or liver, migraine) -
Where this trial is running
Rohtak, Haryana
- Pgids — Rohtak, Haryana, India (Recruiting)
Study contacts
- Study coordinator: Vinay Kumar, MDS
- Email: 29vinaykr@gmail.com
- Phone: 8901149107
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.