To compare the anxiety reducing effect of two oral medicines for uncooperative children during dental procedures
Phase 2
- Registration Number
- CTRI/2023/11/059366
- Lead Sponsor
- Dr Anshula Deshpande
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Children aged between 3-7 years of age.
? Children’s behaviour class I and II according to Frankl behavior rating scale.
? Children with ASA I health status.
? Preoperative heart rate of 80 to 140 beats per minute and Respiratory rate of 24-30 beats
per minute.
? A maximum blood pressure reading of 140/100 mmHg.
? Patients who require LA administration for dental procedures.
Exclusion Criteria
Patient with any chronic systemic illness.
? A history of allergy or intolerance to benzodiazepines.
? Parents who did not give consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ANXIOLYSIS <br/ ><br>PAIN CONTROLTimepoint: 1 WEEK
- Secondary Outcome Measures
Name Time Method PSYCHOMOTOR EFFECTTimepoint: 1 WEEK