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Testing the Efficacy of a Single Dose of Ketorolac and Paracetamol in reducing the pain cause by metal braces treatment procedure in adolescents

Evaluating the Efficacy of a Single Preemptive Dose of Ketorolac and Paracetamol for Managing Orthodontic Procedure Pain in Adolescents: A Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/069011
Enrollment
150
Registered
2024-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: K039- Disease of hard tissues of teeth,unspecified

Interventions

Intervention1: Paracetamol: Patient will receive Single Paracetamol tablet orally (500 mg) 30 min before starting the procedure Intervention2: Ketorol: Patient will receive Single Ketorol tablet orall

Sponsors

Dr Disha khandde
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age: above 14 years weight: above 45 kg Currently undergoing orthodontic treatment with planned procedures requiring moderate pain management (eg. archwire changes) Understanding and willingness to provide informed consent (or parental consent for minors).

Exclusion criteria

Exclusion criteria: History of allergy or hypersensitivity to paracetamol or ketorolac. Currently using any antibiotics or analgesics. Patients with systemic disease, syndromic condition or medically compromised patients.

Design outcomes

Primary

MeasureTime frame
To assess the intensity of pain experienced by the patient during the orthodontic treatment procedure with and without NSAID (Paracetamol and Ketorol) intervention.Timepoint: 4 time points to check intensity of pain: Immediately after the procedure, After 6hr, After 24hr, After 48hr.

Secondary

MeasureTime frame
Which NSAIDs are more effective in controlling the pain caused during the orthodontic treatment procedure Paracetamol or Ketorol.Timepoint: 4 time points to check intensity o pain: immediately after the procedure, 6 hours, 24 hours, 48 hours

Countries

India

Contacts

Public ContactDr Disha Limbraj Khandade

MIDSR Dental College Latur

dishakhandade@gmail.com9370315496

Outcome results

None listed

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