Status:

UNKNOWN

Effect of Cryotherapy Versus Post-operative Ibuprofen Medication on Post-operative Pain in Mandibular Molar Teeth With Symptomatic Irreversible Pulpitis

Lead Sponsor:

Cairo University

Conditions:

Symptomatic Irreversible Pulpitis

Eligibility:

All Genders

18-60 years

Phase:

PHASE1

Brief Summary

Evaluation of the effect of cryotherapy versus post-operative ibuprofen medication on post-operative pain in mandibular molar teeth with symptomatic irreversible pulpitis . a new technique was propos...

Detailed Description

PICO/ Population: Molar teeth with symptomatic irreversible pulpitis. Intervention I: Final irrigation with cold saline (cryotherapy). Intervention II: Ibuprofen post-operative medication. Control: ...

Eligibility Criteria

Inclusion

  • Patients above 18 years old and to 60.
  • Male or female.
  • Patients seeking root canal treatment.
  • Molar teeth with Symptomatic irreversible pulpitis with preoperative sharp, moderate, or severe pain with normal periapical radiographic appearance or slight widening in lamina dura.
  • Systematically healthy patient (ASA I).
  • Patient who can understand VAS and sign informed consent.

Exclusion

  • Medically compromised patients having significant systemic disorders including cardiovascular, respiratory, and gastrointestinal diseases (ASA II, III or IV).
  • History of intolerance to NSAIDS.
  • Patients with two or more adjacent teeth requiring endodontic treatment.
  • External root resorption.
  • Internal root resorption.
  • Vertical root fracture.
  • Periapical lesion.
  • Pregnancy.
  • Use of ibuprofen in the last 12 hour.
  • Bleeding disorder.
  • Long term corticosteroid use. 10
  • Mobility Grade II or III.
  • Pocket depth more than 5mm.
  • Previous root canal therapy.
  • Non-restorability.
  • TMJ problems, bruxism, clenching or traumatic occlusion.
  • Inability to perceive the given instructions.

Key Trial Info

Start Date :

April 1 2022

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

May 1 2023

Estimated Enrollment :

36 Patients enrolled

Trial Details

Trial ID

NCT05341999

Start Date

April 1 2022

End Date

May 1 2023

Last Update

April 22 2022

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