Assessment of Post-Operative Pain After Using Cryotherapy and Dexamethasone
ConditionPost Operative Pain
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-50
SponsorSuez Canal University
About this trial
Evaluation and comparing the effect of cryotherapy and dexamethasone on inflammatory mediators and post-operative pain in symptomatic irreversible pulpitis with acute apical periodontitis.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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)
Disqualifiers
No bleeding upon conducting access preparation.
History of trauma or previous endodontic treatment
Trial design
Design model
Parallel
Treatments tested in this trial
cold NaOCl , dexamethasone
Combination productirrigation solution
NaOCl, dexamethasone
Combination productirrigation solution
cold NaOCl and cold saline
Combination productirrigation solution
NaOCl and saline
Combination productirrigation solution
Treatment groups
60 Participants
are divided into 4 treatment groupsGroup A: cold NaOCl , dexamethasoneExperimental treatment 1 intervention
Group B: NaOCl, dexamethasoneExperimental treatment 1 intervention
Group C: cold NaOCl and cold salineExperimental treatment 1 intervention
Group D: NaOCl and salineActive comparator 1 intervention
Trial outcomes
Primary outcomes
1
post-operative pain
VAS scale (visual analogue scale)
Time frame
7 daysLocations
Sponsors and contacts
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Source ClinicalTrials.gov
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