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Evaluation of Management of Refractory Dentinal Hypersensitivity using partial and complete pulpotomy in Teeth with Dental Erosion: A randomised controlled trial

Comparative effectiveness of partial versus complete pulpotomy for the management of refractory dentinal hypersensitivity in teeth with dental erosion: A randomised clinical trial - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106013
Enrollment
80
Registered
2026-03-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K032- Erosion of teeth

Interventions

Intervention1: Partial Pulpotomy: Partial pulpotomy will be done with the removal of 2-3mm of coronal inflamed pulp, followed by replacement with bio-ceramic material. Intervention2: Complete Pulpotom

Sponsors

Aakash Gupta
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Maxillary permanent teeth with clinically evident dental erosion resulting in dentin exposure. 2. Severe dentinal hypersensitivity, with Schiff Cold Air Sensitivity Scale score more than 2. 3. Teeth scoring 2 or 3 using the BEWE erosion severity index 4. Clinically vital pulp, confirmed by: a. Positive response to cold test b. Absence of spontaneous pain c. Absence of tenderness to percussion 5. Teeth that failed to respond to standardised conservative desensitising therapy after a minimum observation period of more than 3 months. 6. Absence of radiographic signs of pulpal or periapical pathology

Exclusion criteria

Exclusion criteria: 1. Dental caries, restorations, cracks, or structural fractures 2. Attrition-dominant or abrasion-dominant tooth surface loss 3. Signs or symptoms suggestive of irreversible pulp pathology 4. Previous endodontic treatment 5. Periodontal probing depths greater than 4 mm or active periodontal disease 6. Bruxism requiring occlusal splint therapy Patients with systemic conditions affecting pain perception or wound healing 7. Inability to comply with follow-up schedule

Design outcomes

Primary

MeasureTime frame
Dentinal hypersensitivity assessed using the Schiff Cold Air Sensitivity Scale following standardised air blast stimulation (1 s duration, 40 65 psi, 1 cm distance).Timepoint: baseline, 1 month, 3 months, 6 months, and 12 months.

Secondary

MeasureTime frame
1. Pain intensity assessed using the Visual Analogue Scale (VAS) 2. Pulp vitality assessed using cold sensibility testing 3. Postoperative pain & complications 4. Radiographic evaluation for periapical changes 5. Need for further endodontic intervention Timepoint: baseline, 1 month, 3 months, 6 months, & 12 months.

Countries

India

Contacts

Public ContactDr Aakash Gupta

All India Institute of Medical Sciences Bathinda

guptaaakash95@gmail.com09877939523

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026