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Postoperative Pain and Substance P Levels After Bioceramic vs Calcium Hydroxide Intracanal Medicaments in Symptomatic Apical Periodontitis

Study acronym: (BCvsCaOH)
StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Recruitment opened
    • Study sites: 0 to 1
    • Eligibility criteria expanded, about 21 words
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Clinical Evaluation of the Postoperative Pain and Substance P levels Following the use of Bioceramic verses Calcium Hydroxide Intracanal Medicaments in Permanent Mandibular molars with Symptomatic Apical Periodontitis
Trial Details
NCT Number NCT07585721
Lead Sponsor Future University in Egypt
Conditions
(from sponsor)		 Symptomatic Apical Periodontitis
Related terms Postoperative Pain
Enrollment 28 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov