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Comparing the sedative effect of oral lorazepam,promethazine and clonidine sedation of 6-8 years old undergoing dental procedure

Comparative evaluation of the sedative effect of oral lorazepam,promethazine and clonidine sedation of 6-8 year old anxious children undergoing dental treatment-A randomized triple blinded clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/042978
Enrollment
36
Registered
2022-06-02
Start date
Unknown
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Lorazepam: Oral route of administration 2 to 3 mg orally per day Given 2-3 times a day Control Intervention1: Clonidine: Oral route of administration.0.1 mg once a day Control Interven

Sponsors

Dr Simon Jayakumar
Lead Sponsor
S N Venkatesan
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 6-8 years old anxious children undergoing dental treatment

Exclusion criteria

Exclusion criteria: Systemic illness Parents who are not ready to give consent for the study

Design outcomes

Primary

MeasureTime frame
Sedative effect Better reduction of anxietyTimepoint: Within 1-2 hours—

Secondary

MeasureTime frame
Sedative effect Reduction of anxietyTimepoint: Fastest to reduction of anxiety Within 1 hour—

Countries

India

Contacts

Public ContactDr V Ranjith Akshay Seshadri

Saveetha Dental College

mahesh@saveetha.com9840322728

Outcome results

None listed

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