Pulpotomy in primary molars with Propolis and MTA- A 2yr clinical trial
Phase 2
Completed
- Conditions
- Health Condition 1: null- Deep caries lesions without spontaneous or persistent pain
- Registration Number
- CTRI/2018/04/013352
- Lead Sponsor
- KAKARLA SRI ROJA RAMYA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 59
Inclusion Criteria
Primary molars with deep caries lesion without spontaneous or persistent pain and teeth with at least two thirds of root length intact and are restorable with stainless steel crowns in children who are non-allergic to Propolis were included in the study
Exclusion Criteria
Teeth exhibiting the signs and symptoms of chronic infection such as swelling, mobility and sinus tract, teeth showing radiographic evidence of pathologic root resorption, inter-radicular bone loss, periapical pathology and calcifications in the canal were excluded
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method success of Propolis Pulpotomy <br/ ><br>success of Mineral trioxide aggregate PulpotomyTimepoint: success of Propolis Pulpotomy, Time point - 2years <br/ ><br>success of Mineral trioxide aggregate Pulpotomy Time point - 2years
- Secondary Outcome Measures
Name Time Method success of Propolis Pulpotomy <br/ ><br>success of Mineral trioxide aggregate PulpotomyTimepoint: success of Propolis Pulpotomy, Time point - 6 months, 12 months, 24 months <br/ ><br>success of Mineral trioxide aggregate Pulpotomy Time point - 6 months, 12 months, 24 months