Study including trial of pre-emptive analgesia in patient with MIH in which patients having high sensitivity due to low mineralizatio
Phase 2
- Conditions
- Health Condition 1: R00-R99- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified
- Registration Number
- CTRI/2023/09/058044
- Lead Sponsor
- Mira virda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Children with dental hypersensitivity and at least 1st permanent molar affected with hypomineralization
2.Children who are not allergic to analgesics or local anesthesia.
3.The children ranges between 7-10 years.
4.Co-operative children, either positive or definitely positive according to frankel behaviour rating scale.
Exclusion Criteria
1.Non co-operative children
2.The children with amelogenesis imperfecta and dentinogenesis imperfecta
3.The children with history of prolonged bleeding, hypersensitivity or allergic reaction to analgesics
4.The children whose parents have not given concern.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the effectiveness of preemptive analgesia in pain perception in children with molar incisor hypomineralization & hypersensitivity <br/ ><br>Timepoint: pain assesment after local anesthesis, after procedure and 2 hours post operatively
- Secondary Outcome Measures
Name Time Method immediate post operative pain may be reduced & the development of chronic pain may be reduced <br/ ><br>Molar incisor hypomineralization is often accompanied by dental hypersensitivity & difficulty in achieving effective analgesia so to check the effect of preemptive drugs on hypersensitivity in MIH. <br/ ><br> <br/ ><br>Timepoint: After giving local anesthesia, post opertively & 2 hours after procedure