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Oral Preemptive analgesic efficacy in post operative pain , nausea and vomiting in third molar removal surgery - A Randomised control clinical trial

Oral Preemptive analgesic efficacy in post operative pain , nausea and vomiting in third molar removal surgery - A Randomised control clinical trial - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/077104
Enrollment
129
Registered
2024-11-20
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

None listed

Interventions

Intervention1: Analgesic agent: Tablet Aceclofenac + Paractemol and serratiopeptidase Control Intervention1: Nil: Nil

Sponsors

SUURYA KALAA MAKKALL NALANN MARUNDHAGHAM
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients requiring surgical removal of impacted teeth in mandible following by inferior alveolar nerve block

Exclusion criteria

Exclusion criteria: Patient already on analgesics medication, children, patients with peri apical pathology and special care patients.

Design outcomes

Primary

MeasureTime frame
Post operative pain , nausea and vomiting .Timepoint: Post operative pain , nausea and vomiting .

Secondary

MeasureTime frame
Patient’s comfort and general condition post operativelyTimepoint: Patient’s comfort and general condition post operatively

Countries

India

Contacts

Public ContactSunil Yesvanthu S V

Saveetha Dental College and Hospital ,SIMATS

152304004.sdc@gmail.com8778834861

Outcome results

None listed

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