Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07738302

Assessment of Post-Operative Pain After Using Cryotherapy and Dexamethasone

Evaluation and comparing the effect of cryotherapy and dexamethasone on inflammatory mediators and post-operative pain in symptomatic irreversible pulpitis with acute apical periodontitis.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

20 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

sixty patients with single root teeth diagnosed with symptomatic irreversible pulpitis with acute apical periodontitis will be treated in two visits with time interval 72 hrs. Later, they will be randomized into four groups according to the type of irrigant used, group (A): (cold NaOCl , dexamethasone) for 1st visit and cold saline as final rinse for 2nd visit, group (B): ( NaOCl, dexamethasone) for 1st visit and saline as final rinse for 2nd visit (room temperature), group (C): cold NaOCl and cold saline and group D: NaOCl and saline room temperature as control group. Each group will be prepared with trunatomy rotary files according to manufactures instruction. Inflammatory mediators IL-8 and substance P will be assessed by absorbent paper points after access preparation and before obturation using ELISA test. Post-operative pain will be measured after first visit at 6,12, 24,48,72 hrs. then after second visit at 12,24,48,72hrs and 7 days using the visual analogue scale.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Medically free Patients. (ASA I and II)
  • Age between 20-50 years old.
  • Males & Females.
  • Patients' acceptance for participating in the trial through an informed consent (Appendix I)
  • Diagnosed clinically and radiographically with symptomatic irreversible pulpitis with apical peridontitits
  • No periapical radiolucency
  • Patent canals with n

Exclusion criteria

Non restorable teeth.

  • No bleeding upon conducting access preparation.
  • Teeth presenting with:
  • History of trauma or previous endodontic treatment

Treatment and study plan

cold NaOCl , dexamethasone

Combination Product

irrigation solution

NaOCl, dexamethasone

Combination Product

irrigation solution

cold NaOCl and cold saline

Combination Product

irrigation solution

NaOCl and saline

Combination Product

irrigation solution

Primary outcomes

  1. post-operative pain

    Time frame: 7 days

    VAS scale (visual analogue scale)

Sponsors and collaborators

Lead sponsor

Suez Canal University

Other

Registry information

Official study title

Assessment of Post-Operative Pain After Using Cryotherapy and Dexamethasone in Symptomatic Irreversible Pulpitis With Acute Apical Periodontitis: A Randomized Clinical Trial.

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jul 31, 2026
Registry last updated
Jul 31, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.