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Effect of Ibuprofen Sustained Release on Intraoperative and Postoperative Pain in Mandibular Molars

48 participantsStarted 2021-11

Plain-language summary

The study is conducted to evaluate the effect of Ibuprofen sustained release premedication on the success of buccal infiltration anaesthesia, intaroperative pain and post operative pain in mandibular molars with symptomatic irreversible pulpitis and apical periodontitis

Who can participate

Age range18 Years – 50 Years

SexALL

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Inclusion criteria

✓. Systemically healthy patients (ASA I or II).
✓. Patients with Mandibular molar teeth diagnosed with:

Exclusion criteria

✕. Allergy to Ibuprofen
✕. Medically compromised patients having significant systemic disorders. (ASA III or IV).
✕. History of intolerance to NSAIDS.
✕. Patients with two or more adjacent teeth requiring endodontic treatment.
✕. Pregnant or nursing females.
✕. Teeth that have:

What they're measuring

Efficacy of buccal infiltration anaesthesia measured using Visual analogue scale

Timeframe: During root canal treatment procedures

Trial details

NCT IDNCT05053009

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-10

Contact for this trial

Mariam Ah Hossam, B.D.S

01110913251 mariam.ahmed.hosam@dentistry.cu.edu.eg

View on ClinicalTrials.gov More Anesthesia trials