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临床试验/NCT05403125
NCT05403125已完成早期 1 期

Silver Diamine Fluoride: Novel Addition to the Prophylactic Bundle for Dental Management of Radiation-Induced Dental Caries in Oral and Pharyngeal Cancer Patients

Texas A & M University Baylor College Of Dentistry2 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2022年5月20日最近更新:
适应症

试验速览

阶段
早期 1 期
状态
已完成
发起方
入组人数
56
试验地点
2
主要终点
Dental Caries (DMFS)

研究概览

简要总结

The Texas A & M College of Dentistry, with partner Texas Oncology-Baylor Charles A. Sammons Cancer-Center Radiation-Oncology, proposes to conduct a preliminary clinical study (NIH Stage 0) to pilot test a randomized clinical trial of the efficacy of professionally applied 38% silver diamine fluoride to prevent tooth decay in 60 patients who are being treated with radiation for life threatening head and neck cancer.

详细描述

Head and neck cancer has increased in Texas over the last two decades. Radiation-induced tooth decay is a devastating yet potentially preventable side effect of the cancer treatment. Silver diamine fluoride, already the standard of care in children, is inexpensive, easy to apply, and safe. The objective of the research is to conduct a single site pilot RCT (NIH Stage 0) to determine feasibility and preliminarily assess the efficacy of 38% silver diamine fluoride and 5000 PPM fluoride gel for prevention of radiation-induced dental caries over 6 months. Eligible participants will be up to 60 head and neck cancer patients who are scheduled for radiotherapy. The proposed intervention will be applied within 1 m before and at 1- and 3-m post radiation. The primary outcome is dental caries surfaces at 6 months post-radiotherapy (DMFS).Secondary outcomes are The Gingival Index, Gingival Bleeding Index, MDASI-HN, and Oral Health Quality of Life score will be secondary outcomes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

Test and placebo drugs will be identical in appearance and labeled by the manufacturer as A and B. The biostatistician will generate an assignment list. Individual packets will be prepared, and the clinician will open the packet to determine which study drug to apply. The packets and the drug containers will be color coded to minimize error. In each case a second staff member will verify on site that the participant received the correct coded treatment. Blinding: Participants and the examiners will be blind to treatment.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of Head and Neck cancer

排除标准

  • Prognosis less than 1 year
  • Radiation field of treatment does not involve jaws

结局指标

主要结局

Dental Caries (DMFS)

时间窗: 6 months

Dental Caries Surfaces determined by intraoral inspection

次要结局

  • Bleeding Index(6 months)
  • MD Anderson Symptom Inventory-Head and Neck(6 months)
  • Gingival Index(6 months)
  • Oral Health Quality of Life(6 months)

研究者

发起方
Texas A & M University Baylor College Of Dentistry
申办方类型
Other
责任方
Principal Investigator
主要研究者

Amal Noureldin

Clinical Associate Professor

Texas A & M University Baylor College Of Dentistry

研究点 (2)

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