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New Tooth-Filling Material Tested for Treating Deep Cavities in Baby Teeth: A Study Using Checkups and X-Rays

CLINICAL AND RADIOGRAPHICAL EVALUATION OF DIFFERENT HYDROXYAPATITE MATERIALS AS PULPOTOMY AGENT IN PRIMARY MOLARS -AN IN VIVO STUDY - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084631
Enrollment
48
Registered
2025-04-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: K040- Pulpitis

Interventions

Intervention1: Hydroxyapatite (HA) : For all the group samples, hydroxyapatite powder will be mixed with sterile physiological saline solution to achieve a putty like consistency. This mixture will be

Sponsors

sai sushma kallam
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Paediatric patients aged 4 9years. Vital tooth with no history of spontaneous pain, nocturnal pain and provoked pain of longer duration. No clinical evidence of swelling, sinus tract or fistula, mobility and tenderness to percussion. No radiographic evidence of pulp degeneration such as periapical lesion, furcation involvement, pathologic root resorption, internal resorption and pulp calcification. Haemorrhage should stop within 5 minutes from the amputated pulp stump after application of pressure pack.

Exclusion criteria

Exclusion criteria: History of unprovoked tooth ache. Evidence of necrosis or irreversibly damaged pulp. Dystrophic calcification. Primary root lengths less than two third.

Design outcomes

Primary

MeasureTime frame
Clinical Outcome Pain Tenderness on percussion Mobility Swelling Fistulation Time-point(s): 1 month, 3 months, 6 months Radiological Outcome Periodontal ligament widening Furcal radiolucency External resorption Internal resorption Time-point(s): 1 month, 3 months, 6 months Comparative Clinical and Radiological Outcome Comparison of clinical and radiological outcomes of different hydroxyapatite materials at 1, 3 & 6 months Timepoint: 1, 3 and 6 months

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public Contactsai sushma kallam

Sibar Institute of Dental Sciences.

kakarlapranitha@gmail.com9441818713

Outcome results

None listed

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