Endodontic Treatment of participants aged 3 to 9 years with pain in their teeth suitable material and to assess the outcome on clinical and radiographic parameters

MTA pulpotomy/pulpectomy in vital primary teeth with symptoms of irreversible pulpitis-A randomized control Trial - NIL

Status

Active, not recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/087901

Enrollment

Registered

2025-05-30

Start date

Unknown

Completion date

Unknown

Last updated

2025-06-24

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: MTA and Endoflas: Vital primary teeth with symptoms of irreversible pulpits will be randomly allocated using chit method in either pulpotomy or pulpectomy group. Control Intervention1:

Eligibility

Inclusion criteria

Inclusion criteria: 1. History of pain in primary molar 2. Healthy (ASA I and II) co-operative children of age 3-9 years. 3. Pulpally involved vital deeply carious vital primary molars. 4. If haemostasis is achieved within 10 minutes (3,6,8,10 minutes) on application of pressure after deep removal of coronal pulp.

Exclusion criteria

Exclusion criteria: 1. Clinical evidence of mobility and pulp necrosis 2. Swelling and Periradicular abscess. 3. Radiological signs of internal/external resorption. 4. Any radiographic evidence of periapical pathology.

Design outcomes

Primary

Measure	Time frame
1.Assessment of bleeding time at root canal orifices after removal of coronal pulp in all the primary molars undergoing pulpectomy/pulpotomy 2.To evaluate clinical parameters at pre-operative, post operative (immediately after procedure), 1 month, 3 months and 6 months period along with radiographic parameters at pre-operative, postoperative (immediately after procedure) and 6 months follow up in treated primary molars. Timepoint: 1. Bleeding time will be assessed at 3,6,8,10 minutes 2. Radiographic parameters will be assessed 1 month, 3 months and 6 months 3. Clinical parameters will be assessed 1 month, 3 months and 6 months	—

Measure

Time frame

1.Assessment of bleeding time at root canal orifices after removal of coronal pulp in all the primary molars undergoing pulpectomy/pulpotomy 2.To evaluate clinical parameters at pre-operative, post operative (immediately after procedure), 1 month, 3 months and 6 months period along with radiographic parameters at pre-operative, postoperative (immediately after procedure) and 6 months follow up in treated primary molars. Timepoint: 1. Bleeding time will be assessed at 3,6,8,10 minutes 2. Radiographic parameters will be assessed 1 month, 3 months and 6 months 3. Clinical parameters will be assessed 1 month, 3 months and 6 months

—

Secondary

Measure	Time frame
NILTimepoint: NIL	—

Countries

India

Contacts

Public ContactDr Vibhusha Jain

SGT Dental College, Gurgaon Haryana

shaloosandeep@gmail.com9215668621

Outcome results

None listed

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