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Different Hemostatic Agents Used in Partial Pulpotomy on Pulp Survival and Postoperative Pain

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Trial status: Not Yet Recruiting to Recruiting
    • Primary completion date changed from estimate of Feb 1, 2026 to Nov 1, 2025
    • Study completion date: Aug 1, 2026 to May 1, 2026
    • Start date changed from estimate of Aug 1, 2025 to May 1, 2025
    v4
  2. Re-verified, no change to tracked fieldsv3
  3. Start date: Jul 1, 2025 to Aug 1, 2025
    • Primary completion date: Jan 1, 2026 to Feb 1, 2026
    • Study completion date: Jul 1, 2026 to Aug 1, 2026
    v2
  4. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
This randomized clinical trial evaluates the efficacy of sodium hypochlorite (NaOCl), chlorhexidine (CHX), and cold saline as hemostatic agents in partial pulpotomy. The study compares postoperative pain (via VAS scores) and pulp survival (via clinical/radiographic evaluation) at 1, 3, 7 days, 6 months, and 12 months
Trial Details
NCT Number NCT07058727
Lead Sponsor Cukurova University
Conditions
(from sponsor)		 Efficacy of Hemostatic Agents, Partial Pulpotomy, Postoperative Pain
Related terms Postoperative Pain
Enrollment 75 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov