Different Hemostatic Agents Used in Partial Pulpotomy on Pulp Survival and Postoperative Pain
Recruiting
N/A
Interventional Study
Efficacy of Hemostatic Agents
Partial Pulpotomy
Postoperative Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 15 – 55
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 75 (estimated)
- Sponsor
- Cukurova University · Other
Who this trial is looking for
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About This Trial
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 Locations
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Eligibility Criteria
Inclusion Criteria:
* Permanent teeth with carious pulp exposure (no spontaneous pain).
* Positive vitality test (Endo-Ice).
* No periapical radiolucency.
Exclusion Criteria:
* Systemic diseases affecting healing.
* Pregnancy.
* Non-vital pulp/necrosis
Inclusion Criteria:
* Permanent teeth with carious pulp exposure (no spontaneous pain).
* Positive vitality test (Endo-Ice).
* No periapical radiolucency.
Exclusion Criteria:
* Systemic diseases affecting healing.
* Pregnancy.
* Non-vital pulp/necrosis
Contacts
No contact information available.