- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT03616327
Workflow Validation of an In-Home Feedback Controlled Mandibular Positioner
연구 개요
상세 설명
Sleep apnea (OSA) is a condition in which the air passage in the throat closes or partly closes during sleep and repeatedly interrupts breathing. The standard treatment of sleep apnea is continuous positive airway pressure (CPAP) applied to the nose, but it is not suitable for all patients. Another treatment is to use an oral appliance in the mouth during sleep. The appliance covers the upper and lower teeth and acts to pull the lower jaw forward, opening the throat passage and allowing normal breathing.
Oral appliance treatment does not treat sleep apnea effectively in all patients. In order to identify those patients for whom oral appliance therapy will work, Zephyr Sleep Technologies has invented a remotely controlled device that tests various positions of the lower jaw. This commercially available device, known as MATRx, is an FDA-cleared motorized dental positioner that can be used in an overnight sleep study performed in the hospital or clinic. Temporary dental-impression trays cover the upper and lower teeth. These are attached to a small motor that slowly and gently pulls the lower jaw forward under the control of a technician who determines when the best position is reached. Knowing the best position, and the likelihood of future success, allows the dentist to build an oral appliance with confidence.
In order to eliminate the need for an overnight in-hospital sleep study, Zephyr Sleep Technologies has invented a new investigational device that allows clinicians to decide whether or not an individual is likely to benefit from oral appliance therapy, from the comfort of the individual's own home. An investigational device is one that is not cleared by the U.S. Food and Drug Administration (FDA). Like the MATRx, the patient sleeps with a motorized positioner that moves the lower jaw. However, the new device (called MATRx plus) is automatically controlled by a computer, rather than a sleep technician, making it a feedback controlled mandibular positioner. Participation in this study will provide important data regarding the use of these device in their intended commercial setting, the dentist's office.
Zephyr has previously carried out three research studies leading to the development of this feedback controlled mandibular positioner. The first study showed that the technician controlled positioner was able to accurately identify patients suitable for oral-appliance therapy, i.e., those with a good likelihood of success with a permanent device.
This study also identified the amount of jaw protrusion (how far forward the lower jaw needs to be pulled) that will provide therapeutic relief of the patients' sleep apnea. This trial resulted in the placement of the device on the market, now sold in the United States as MATRx. The second two trials showed that the feedback controlled software used by the new positioner was very accurate and was able to identify successful candidates in a home setting.
No serious or permanent problems or risks were identified in any of these research studies. Participants reported minor tooth and gum discomfort on the morning following the test and other minor issues including canker sores, excess saliva and being unable to sleep. Since other studies were designed to establish the safety and efficacy of the device, the purpose of the present research study is to collect additional data regarding the workflow of the device as it would occur during commercial use.
The test will occur over a series of nights in the home or during a single night in the sleep laboratory. The test type will be decided by the care providers and this study will only document the rationale and will not influence the choice of test. Participants will be asked to provide feedback as to the preferred test, and will be told if they are candidates for oral appliance therapy based on the output of the test.
연구 유형
등록 (실제)
단계
- 해당 없음
연락처 및 위치
연구 장소
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North Carolina
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Charlotte, North Carolina, 미국, 28207
- Charlotte Oral Surgery
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Minimum 18 years of age
- Participant has been deemed suitable for oral appliance therapy
- Adequate mandibular range of motion
- Adequate dentition
- Ability to understand and provide informed consent
- Ability and willingness to meet the required schedule
Exclusion Criteria:
- Loose teeth or advanced periodontal disease
- Full dentures
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 다른
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
---|---|
다른: MATRx in-lab or MATRx plus test
Participants will undergo the MATRx in-lab or MATRx plus home test to determine adequacy for mandibular repositioning oral appliance therapy.
The tests only differ in their setting (i.e., in the sleep lab or at home).
All participants will receive the same treatment protocol preceding and following the MATRx/MATRx plus test.
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The MATRx remotely controlled mandibular positioner (RCMP) consists of temporary dental trays connected to an extra-oral linear actuator that protrudes the mandible.
MATRx is used during polysomnography, where sleep and cardio-respiratory variables are recorded during sleep.
The position of the mandible is controlled remotely by a sleep technologist, who moves the mandible while monitoring cardio-respiratory variables.
The test determines if mandibular protrusion eliminates pharyngeal obstruction and the required protrusion.
The MATRx plus is used in the home.
Like the RCMP, the patient sleeps with the motorized mandibular positioner (MP) in place.
However, the MP's position is controlled by a computer, making it a feedback controlled mandibular positioner (FCMP).
The FCMP detects apneas and hypopneas in real time.
Using this information, the controller decides when to move the mandible and by how much.
The test predicts of therapeutic outcome with OA and provides a target protrusion.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
---|---|---|
Feasibility of MATRx plus use in a dental sleep medicine practice, as determined by successful completion of test
기간: 1 week
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Evaluation of the process to effectively coordinate the respective roles in the deployment of the sleep test.
Feasibility will be determined by the ability for patients to complete the MATRx plus test.
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1 week
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
---|---|---|
Patient satisfaction of test, as determined by feedback from the patients following the test.
기간: 1 week
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Questionnaire on patient preference and feedback with respect to the test.
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1 week
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공동 작업자 및 조사자
수사관
- 수석 연구원: Kent Moore, DDS, MD, Charlotte Oral Surgery
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- ZCP201705
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
미국에서 제조되어 미국에서 수출되는 제품
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
MATRx in-lab, MATRx plus에 대한 임상 시험
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Zephyr Sleep Technologies완전한
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Klein Buendel, Inc.National Institute on Alcohol Abuse and Alcoholism (NIAAA); Pacific Institute for Research...모병