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
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
75
2.5% NaOCl applied for 1 min to exposed pulp for hemostasis, followed by standard pulp capping
2% CHX applied for 1 min to achieve hemostasis, with identical subsequent steps to NaOCl group
Hemostasis via 4°C saline (1 Min), then standardized pulp capping
Çukurova Üniversitesi Diş Hekimliği Fakültesi
Adana, Sarıçam, Turkey (Türkiye)
RECRUITINGPostoperative Pain
The patient will be asked to rate the pain on the 1st, 3rd and 7th day according to VAS. (The patient is asked to score their pain in this range, with 0 being the lowest and 10 being the highest.)
Time frame: 1 week
Pulp Survival Rate
The pulp is expected to be vital, without percussion tenderness and without spontaneous pain
Time frame: 12 months
Clinical Success
Maintaining the integrity of the restoration No need for endodontics treatments
Time frame: 12 months
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