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临床试验/NCT02941276
NCT02941276已完成不适用

Long-term Evaluation of the Effectiveness Of a Novel Intra-oral Electro-stimulator for the Treatment of raDiotherapy-ASsociated Dry Mouth

University College, London0 个研究点目标入组 84 人开始时间: 2011年11月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
84
主要终点
Improvement of subjective perception of dry mouth as measured on the Visual Analog Scale

研究概览

简要总结

This trial is looking at using an intra-oral electrostimulating device for the management of radiotherapy-induced dry mouth.

详细描述

Dry mouth is a common complaint of radiotherapy for cancer of the head and neck region. It is a distressing often persistent condition which can lead to longlasting oral discomfort, dental infections, diminished quality of life, social isolation and loneliness. Unfortunately, current therapies of dry mouth are often unsatisfactory, expensive and may result in adverse effects. A novel intraoral electronic device has recently been developed to treat dry mouth. The device, acting as a "salivary pacemaker", harmlessly stimulates nerves of the salivary glands and does not cause adverse side effects. The aim of this proposal is to assess the longterm effects of such a device in this population, which have yet to be investigated, to demonstrate whether its daily application is an effective method of lessening dry mouth and improving life quality. 84 individuals will be enrolled in the study to use the device for 12 months, after receiving appropriate instructions. 42 participants (out of 84) will act as controls as they will receive a sham device that will not deliver electric stimuli but only tactile stimulation (like using a chewing gum). All participants will be allowed to continue using their routine local therapy for dry mouth (e.g. artificial saliva) during the study. Each participant will keep a diary relevant to the frequency of use and potential changes in dry mouth sensation. Participants will also be asked to attend hospital appointments to measure changes in saliva production and complete questionnaires on their dry mouth and quality of life. The device has the potential to radically change current clinical practice. If the trial is successful, the use of the device will provide patients having radiation-induced dry mouth with a safe and drug-free therapeutic modality.

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
Triple (Participant, Investigator, Outcomes Assessor)

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

  • To be at least 18 years old
  • To have received more than 40 Gy of external beam RT for cancer in the H&N region at least 4 months before entry into the study
  • To have grade 1 or 2 of RTOG/EORTC Late Radiation Morbidity Scoring Schema
  • To have a degree of minimum degree of dryness of 50mm (≥50mm) on a 100mm VAS scale (0=no dryness; 100
  • =maximum dryness).
  • To have demonstrable residual salivary gland function (increase in salivary flow on appropriate stimulation (e.g. chewing paraffin wax)
  • To have at least one parotid gland

排除标准

  • To have severe uncontrolled systemic disease (on the basis of the classification of the American Society of Anesthesiology: ASA IV and ASA V)
  • To have known allergy to materials similar to those used in the investigational product
  • To wear other active implants such as cardiac pacemaker or defibrillator, or hearing aids
  • To have an unstimulated whole salivary flow of 0ml/15min (complete absence of unstimulated salivary flow as measured via sialometry for 15 minutes).
  • To use of pilocarpine as systemic therapy
  • To have grade 3 RTOG/EROTC or no resting saliva (sialometry = 0mL/1.5 min)
  • To have no parotid glands

结局指标

主要结局

Improvement of subjective perception of dry mouth as measured on the Visual Analog Scale

时间窗: 12 month

The primary outcome is defined as the proportion of patients reporting a 30% reduction of xerostomia symptoms as evaluated through a 100mm VAS (100mm=maximum dryness).

次要结局

  • Participant compliance(12 month)
  • Head and Neck cancer Quality of Life(12 month)
  • Oral Health Quality of Life(12 month)
  • General quality of Life(12 month)
  • Salivary function(12 month)

研究者

申办方类型
Other
责任方
Sponsor

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