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Comparison of the Pain Levels of Single-Dose Premedication With Piroxicam and Prednisolone on Post-Endodontic Pain in Single-Visit Root Canal Treatment of Premolars

R

RANA AHMAD

Status and phase

Not yet enrolling
Phase 4

Conditions

Irreversible Pulpitis With Apical Periodontitis
Symptomatic Apical Periodontitis

Treatments

Drug: piroxicam 20mg
Drug: Group B: patients will be given prednisolone 20mg as premedication

Study type

Interventional

Funder types

Other

Identifiers

NCT07281807
TUF/IRB/28/2025

Details and patient eligibility

About

To compare the post operative mean pain scores by administering single-dose preoperative piroxicam and prednisolone in patients of irreversible pulpitis with symptomatic apical periodontitis.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy patient ranging between 18-40 years
  • Having at least one premolar with diagnosis of symptomatic irreversible pulpitis according to history, examination and radiographs.
  • Teeth having mature apex confirmed by periapical radiographs.

Exclusion criteria

  • History of systemic disorders including HIV, Hepatitis

    • Pregnancy (As per Medical record/ Verbally)
    • Patient using medication such as analgesics or anti-inflammatory drugs
    • Patient allergic to lignocaine, piroxicam and prednisolone
    • Tooth not suitable for restoration
    • Periodontal probing depth ≥ 4mm
    • Retreatment cases
    • Patients having calcified canals assessed by radiographic findings

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Double Blind

60 participants in 2 patient groups

Group A: piroxicam
Experimental group
Description:
Group A: patients will be given piroxicam 20mg as premedication
Treatment:
Drug: piroxicam 20mg
Group B: prednisolone
Active Comparator group
Description:
Group B: patients will be given prednisolone 20mg as premedication
Treatment:
Drug: Group B: patients will be given prednisolone 20mg as premedication

Trial contacts and locations

0

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Central trial contact

rana ahmad, B.D.S., F.C.P.S.

Data sourced from clinicaltrials.gov

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