Partial pulpotomy in mature lower molars with SIP using calcium hypochlorite vs sodium hypochlorite
Official title: Outcome of Partial Pulpotomy in Permanent Mandibular Molars With Symptomatic Irreversible Pulpitis After Wound Lavage With Calcium Hypochlorite or Sodium Hypochlorite
Run by Postgraduate Institute of Dental Sciences Rohtak · NCT07748676 · Data updated 2026-11-12
This trial tests whether washing the exposed pulp with calcium hypochlorite or with sodium hypochlorite during partial pulpotomy in adults helps healing and reduces pain.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 40 Years |
| Sex | All |
| Enrollment | 106 (estimated) |
| Sponsor | Postgraduate Institute of Dental Sciences Rohtak Academic / other |
| Locations | 1 site (Rohtak, Haryana) |
| Status | Recruiting |
| Started | April 29, 2026 |
| Main results expected | October 28, 2027 |
| Study ends | October 28, 2027 |
| Registry record updated | August 26, 2026 |
| Trial ID | NCT07748676 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18–40 with mature permanent mandibular molars, extremely deep caries, SIP, and PAI score ≤ 2.
✕Probably not a fit
Patients with non-restorable teeth, necrotic pulp, sinus tract, swelling, or radiographic root resorption may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized trial compares two wound lavage solutions, 2.5% calcium hypochlorite and 2.5% sodium hypochlorite, used after removing a small portion of inflamed pulp in mature permanent mandibular molars with symptomatic irreversible pulpitis. Outcomes include clinical and radiographic success at 6 and 12 months, as well as patient-reported pain and oral health-related quality of life over time. Eligibility focuses on adults 18–40 with deeply carious, restorable molars and controlled inflammation. The study aims to determine which lavage agent better supports pulpal healing while preserving tooth structure. It is conducted at PGIDS Rohtak with a randomized allocation to the two intervention arms.
Why it matters
Potential benefit: If successful, one solution could become the preferred lavage agent to improve healing and patient experience after partial pulpotomy.
How similar studies have gone: Partial pulpotomy has shown promise in irreversible pulpitis, but direct comparisons of lavage agents are limited, making this approach relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. patients aged 18-40 years 2. Mature permanent mandibular molars with extremely deep caries (caries penetrating the entire thickness of the dentine radiographically, without radiopaque zone separating lesion from the pulp) and clinical diagnosis of SIP with PAI score ≤ 2 3. Periodontally healthy teeth (probing pocket depth ≤3 mm and mobility within normal limit) 4. Patients having physical status of class 1 or 2 according to ASA classification 5. Pulpal bleeding could be controlled within 10 min following pulp amputation Exclusion Criteria: 1. Non restorable teeth 2. No pulp exposure even after complete caries excavation 3. Necrotic or partially necrotic pulp upon exposure 4. Presence of sinus tract or soft tissue swelling 5. Radiographic signs of internal or external root resorption 6. Pregnant women
Where it's running
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Pgids
Rohtak, Haryana, India Recruiting
Study contacts
- Principal investigator: Dr Mayank Arora, MDS — PGIDS, Rohtak, 124001
- Study coordinator: Dr. Mayank Arora, MDS
- Email: dr.arora002@gmail.com
- Phone: +918295964200
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.