Study of the Effectiveness of Cevimeline on Oral Health in Patients With Radiation Induced Xerostomia - Full Text View

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 4


Study Type:	Interventional
Study Design:	Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver) Primary Purpose: Treatment
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

Resource links provided by NLM:

Genetics Home Reference related topics: head and neck squamous cell carcinoma

MedlinePlus related topics: Dental Health Dry Mouth

Drug Information available for: Cevimeline hydrochloride Cevimeline

U.S. FDA Resources

Further study details as provided by American Academy of Otolaryngology-Head and Neck Surgery Foundation:

Primary Outcome Measures:

To assess the impact of increased salivary flow due to treatment with cevimeline compared to placebo in patient reported oral health using the OHIP-49 [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:

To evaluate if increased salivary flow due to cevimeline treatment results in improved patient reported quality of life using the UW-QOL-HN [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]
To evaluate which subscales of the OHIP-49 are improved most by increased salivary flow due to cevimeline treatment [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]
To evaluate which subscales of the UW-QOL-HN are improved most by increased salivary flow due to cevimeline treatment [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]


Enrollment:	54
Study Start Date:	May 2007
Study Completion Date:	August 2009
Primary Completion Date:	June 2009 (Final data collection date for primary outcome measure)

Arms	Assigned Interventions
Experimental: Cevimeline Evoxac tid for xerostomia	Drug: Cevimeline Other Name: evoxac
Placebo Comparator: Placebo sugar pill	Drug: Cevimeline Other Name: evoxac

Detailed Description:

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 (Adult, Senior)
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Subject is at least 18 years old and able to give written informed consent
Subject has received external beam radiotherapy > 4000 cGy for SCCA of the head and/or neck
Radiation therapy was completed at least 16 weeks (4 months) prior to enrollment into the study but not greater than 52 weeks (12 months)
Radiation included at least three of four of the major salivary glands (submandibular and parotid glands) in the initial field (boost fields may or may not include the parotid gland)
Primary therapy was designed with curative intent. Surgery is permitted if the remaining inclusion criteria are met
Grade 1 or 2 xerostomia by CTC version 3.0 criteria (Appendix D)
Demonstratable salivary flow as assessed by the clinician after administration of a potent sialogogue such as lemon juice (1 teaspoon)
Subject has at least one anatomically intact parotid gland and one submandibular gland
ECOG performance status of 0, 1, or 2
An EKG obtained has been performed in the past 6 months showing no arrhythmias or contraindication to administration of a muscarinic agent AND there has been no interval change in cardiac health
Subject is able to eat an oral diet to maintain adequate hydration and nutrition
Subject has provided informed consent
Subject is English speaking and of sufficient mental capacity to comply with the study requirements
Female subjects of child bearing potential have a negative serum pregnancy test and agree to use an approved method of birth control

Exclusion Criteria:

Subject has a life expectancy less than 12 months.
Subject is known or suspected to have persistent disease after curative intent
Subject is greater than 12 months out from completion of radiation therapy
Subject is pregnant or nursing
Subject had previous cancer of the head and/or neck and is being treated with a second course of radiation therapy
Subject has a history of an autoimmune disease with pretreatment xerostomia (i.e. Sjogrens) or other underlying systemic illness known to cause xerostomia independent of prior radiation therapy exposure
Subject has had resection of both parotid glands
Subject has history of cardiomyopathy or untreated moderate to severe CAD
Subject has known cardiac arrhythmias
Subject has grade 3 xerostomia (CTC v.3)or no demonstratable salivary flow after the test dose by visual inspection
Subject has history of significant renal or hepatic impairment
Subject uses a gastrostomy tube for nutrition supplementation
Subject is taking medications specified in Appendix C
Subject is taking or has taken any investigational new drug within the last 30 days or is planning to take such a drug during the course of this study
Subject has a contraindication to administration of muscarinic medications.
Subject has been treated previously with a muscarinic agent for xerostomia (i.e., Pilocarpine HCl)

Contacts and Locations

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00466388

Locations


United States, Colorado

Colorado Springs, Colorado, United States
United States, Illinois
Carle Clinic Association
Urbana, Illinois, United States, 61801
United States, Kansas
University of Kansas Medical Center
Kansas City, Kansas, United States, 66160
United States, Kentucky
Commonwealth Ear, Nose and Throat
Louisville, Kentucky, United States, 40207
United States, Pennsylvania
Associated Otolaryngologist
Palmyra, Pennsylvania, United States, 17078
University of Pittsburgh
Pittsburgh, Pennsylvania, United States, 15213
United States, Virginia
Fauquier ENT Consultants
Warrenton, Virginia, United States, 20186

Sponsors and Collaborators

American Academy of Otolaryngology-Head and Neck Surgery Foundation

Duke University

Investigators


Principal Investigator:	David Witsell, MD	Duke University

More Information


Responsible Party:	American Academy of Otolaryngology-Head and Neck Surgery Foundation
ClinicalTrials.gov Identifier:	NCT00466388 History of Changes
Other Study ID Numbers:	AAO-101
Study First Received:	April 23, 2007
Last Updated:	May 21, 2014
Health Authority:	United States: Institutional Review Board

Keywords provided by American Academy of Otolaryngology-Head and Neck Surgery Foundation:


dry mouth

Additional relevant MeSH terms:


Xerostomia Salivary Gland Diseases Mouth Diseases Stomatognathic Diseases Cevimeline Parasympathomimetics Autonomic Agents	Peripheral Nervous System Agents Physiological Effects of Drugs Muscarinic Agonists Cholinergic Agonists Cholinergic Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action

ClinicalTrials.gov processed this record on September 28, 2016

Study of the Effectiveness of Cevimeline on Oral Health in Patients With Radiation Induced Xerostomia (SMILE)