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| Sponsor: | American Academy of Otolaryngology-Head and Neck Surgery Foundation |
|---|---|
| Information provided by: | American Academy of Otolaryngology-Head and Neck Surgery Foundation |
| ClinicalTrials.gov Identifier: | NCT00466388 |
Purpose
The purpose of this study is to determine the effectiveness of cevimeline (versus placebo) on the oral health of patients who have dry mouth which was caused by radiation therapy that was given for treatment of head and/or neck cancer.
| Condition | Intervention | Phase |
|---|---|---|
|
Xerostomia |
Drug: Cevimeline |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study |
| Official Title: | An Investigator-Initiated,Multicenter,Randomized,Double-Blind Placebo-Controlled Design Study to Assess the Effectiveness of CeviMeline to Improve OraL Health in Patients With XErostomia Secondary to Radiation Therapy for Treatment of Head and Neck Squamous Cell Carcinoma |
| Estimated Enrollment: | 108 |
| Study Start Date: | May 2007 |
| Estimated Study Completion Date: | November 2008 |
Treatment of advanced head and neck squamous cell carcinoma (SCCA) requires aggressive therapy often combining surgical interventions with radiation therapy. Besides surveillance for persistent or recurrent cancer, clinicians seek to help minimize the side effects resulting from these aggressive treatments. Xerostomia, or "dry mouth", impacts each patient's long term health and quality of life due to the significant and diverse health consequences of having too little saliva. Normal swallowing, speaking, resistance to infection, and taste acuity are health domains that are affected by dry mouth. Psycho-social functioning decreases for many of these patients due to the extra effort to communicate and socialize (Locker D 2004).
Xerostomia is often a consequence of radiation treatment (XRT), especially when the XRT fields encompass the parotid glands and submandibular glands bilaterally. The disability and consequences of xerostomia extend beyond dysphagia, poor appetite secondary to difficulty of mastication, and loss of taste (Chambers et al. Xerostomia 2004). Since saliva is essential to normal oral flora and healthy teeth, the lack of saliva in these patients can dramatically and rapidly result in a decline of the patient's oral health. Dental complications can occur and present significant ongoing medical and surgical problems.
Our study proposes to use the Oral Health Impact Profile, OHIP-49, to measure disease-specific quality of life and functional outcomes due to radiation related xerostomia in head and neck cancer patients. The evaluation of patient QOL concomitantly with patient functioning as proposed in the SMILE protocol is an "evidence study to evaluate treatment effectiveness". The use of patient-oriented outcome measures are increasingly important to health insurers and government, but these measures are also aligned with the World Health Organization's mandate that health is a resource to manage which must be utilized and preserved so that individuals experience and gain satisfaction from living (Epstein J.1986). The OHIP-49 is patient reported outcome measure which is publicly available, validated in adult populations world-wide, and can be used an effectiveness measure. The questions are easy to answer and are based upon a 5 level likert type scale reflecting frequency of "bother" within individual psychosocial domains.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: David Witsell, MD | 919-668-8680 | david.witsell@duke.edu |
| Contact: Tasha Carmon, BA | 919-668-8385 | tasha.carmon@duke.edu |
| United States, Colorado | |
| Recruiting | |
| Colorado Springs, Colorado, United States | |
| United States, Illinois | |
| Carle Clinic Association | Recruiting |
| Urbana, Illinois, United States, 61801 | |
| United States, Kansas | |
| University of Kansas Medical Center | Recruiting |
| Kansas City, Kansas, United States, 66160 | |
| United States, Kentucky | |
| Commonwealth Ear, Nose and Throat | Recruiting |
| Louisville, Kentucky, United States, 40207 | |
| United States, Pennsylvania | |
| Associated Otolaryngologist | Recruiting |
| Palmyra, Pennsylvania, United States, 17078 | |
| University of Pittsburgh | Recruiting |
| Pittsburgh, Pennsylvania, United States, 15213 | |
| United States, Virginia | |
| Fauquier ENT Consultants | Recruiting |
| Warrenton, Virginia, United States, 20186 | |
| Principal Investigator: | David Witsell, MD | Duke University |
More Information
| Study ID Numbers: | AAO-101 |
| Study First Received: | April 23, 2007 |
| Last Updated: | August 24, 2007 |
| ClinicalTrials.gov Identifier: | NCT00466388 History of Changes |
| Health Authority: | United States: Institutional Review Board |
|
dry mouth |
|
Mouth Diseases Parasympathomimetics Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Cholinergic Agonists Physiological Effects of Drugs Cholinergic Agents Xerostomia |
Pharmacologic Actions Cevimeline Autonomic Agents Muscarinic Agonists Stomatognathic Diseases Peripheral Nervous System Agents Salivary Gland Diseases |