The Effect of Different Hemostatic Agents Used in Partial Pulpotomy on Pulp Survival and Postoperative Pain: A Randomized Clinical Trial
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 75
- 主要终点
- Postoperative Pain
研究概览
简要总结
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
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 15 Years 至 55 Years（Child, Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Permanent teeth with carious pulp exposure (no spontaneous pain).
- •Positive vitality test (Endo-Ice).
- •No periapical radiolucency.
排除标准
- •Systemic diseases affecting healing.
- •Pregnancy.
- •Non-vital pulp/necrosis
研究组 & 干预措施
Arm 1
2.5% NaOCl applied for 1 min after pulp exposure.
干预措施: Sodium Hypochlorite 2,5% (Drug)
Arm 2
2% CHX applied for 1 min
干预措施: Chlorhexidine (Drug)
Arm 3
Hemostasis achieved with 4°C saline for 1 min.
干预措施: Cold Saline (Drug)
结局指标
主要结局
Postoperative Pain
时间窗: 1 week
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.)
Pulp Survival Rate
时间窗: 12 months
The pulp is expected to be vital, without percussion tenderness and without spontaneous pain
次要结局
- Clinical Success(12 months)
研究者
Zehra SUSGUN YILDIRIM
Principal Investigator
Cukurova University