DRKS00030346已完成未知
Investigation of matrix metalloproteinase-9 levels in dental pulp blood as a marker for the inflammatory state of the pulp tissue - a prospective clinical pilot study
Poliklinik für ZahnerhaltungskundeUniversitätsklinikum Heidelberg0 个研究点目标入组 44 人开始时间: 2022年10月25日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 44
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomized controlled study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 12 Years 至 one(—)
- 性别
- All
入选标准
- •Male and female patients of the age = 12 years
- •- Patients from the Department of Conservative Dentistry at Clinic for Oral, Dental and Maxillofacial Diseases, University Hospital Heidelberg or from one of the cooperating trial centres
- •- Present declaration of consent of the patient to participate in the study; in the case of underage patients, the consent of the legal guardian/legal representative must also be present
- •- Adult patients must be able to give consent
- •- Teeth in which (the clearly vital) pulp of a tooth with a caries extending into the pulp resulting in pulp exposure during caries excavation.
- •- The pulp tissue of the treated tooth must be classified either as completely asymptomatic, reversibly inflamed (reversible pulpitis) or irreversibly inflamed (irreversible pulpitis).
- •- The tooth must be treatable and restorable under rubber dam isolation.
- •- The restoration of the tooth after partial pulpotomy and subsequent direct pulp capping with ProRoot MTA® using composite must be completed within 24 hours.
排除标准
- •- Primary teeth
- •- Patients whose state of health is reduced to such an extent that they are not able to cope with the usual stress (e.g. immunocompromised patients)
- •- Patients for the period of their pregnancy
- •- Patients who have not yet reached the age of 12
- •- Patients who do not give their consent to participate in the study
- •- Patients who have taken antibiotics in the last four weeks
- •- Patients who have taken medicaments with a potential influence on the MMP-9 level, e.g. bisphosphonates, statins, acetylsalicylic acid (exception is group 3, in which patients have taken the NSAID Ibuprofen)
- •- Teeth that have a longitudinal fracture at the time of the treatment with partial pulpotomy
- •- Teeth which, at the time of the treatment, showed bone loss down to the apical third of the root, teeth with a perio-endo-lesion or teeth with a degree of mobility of 3
- •- Teeth that showed at the periapical radiograph a periapical index PAI=2 at the day of the treatment (arm 1 and 2 with partial pulpotomy)
- •- Teeth that showed at the periapical radiograph a periapical index PAI>2 at the day of the treatment (arm 3 and 4 with root canal treatment). Teeth in which an internal or external tooth/root resorption is already evident at day of the treatment with partial pulpotomy,
- •- Teeth that could not be assigned unequivocally to one of the four diagnostic groups after clinical and radiographic examination
研究者
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