Actively Recruiting

Phase Not Applicable
Age: 15Years - 55Years
All Genders
NCT07058727

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

Led by Cukurova University · Updated on 2026-04-01

75

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

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

Who Can Participate

Age: 15Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Permanent teeth with carious pulp exposure without spontaneous pain
  • Positive vitality test using Endo-Ice
  • No periapical radiolucency
Not Eligible

You will not qualify if you...

  • Presence of systemic diseases affecting healing
  • Pregnancy
  • Non-vital pulp or pulp necrosis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Çukurova Üniversitesi Diş Hekimliği Fakültesi

Adana, Sarıçam, Turkey (Türkiye), 01250

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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