Terminé

Salivary Evaluation in Healthy Volunteers

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Ce qui est collecté

Collecte de données

Qui peut participer

Healthy

+ Salivary Gland Disease
De 18 à 70 ans
Comment se déroule l'étude

Autre

Observationnel
Date de début : octobre 1993

Résumé

Sponsor principalNational Institute of Dental and Craniofacial Research (NIDCR)
Dernière mise à jour : 24 septembre 2018
Issu d'une base de données validée par les autorités. Revendiquer cette étude
Date de début de l'étude : 26 octobre 1993Date à laquelle le premier participant a commencé l'étude.

Saliva is critical in maintaining oral health and comfort. Our laboratory has investigated several disorders of salivary glands. The purpose of this protocol is to obtain data from healthy volunteers for comparison with data from patients with salivary dysfunction. We plan to utilize the NIH Clinical Center Clinical Research Volunteer Program to solicit paid participation from healthy adults. Study procedures are accomplished in 2-3 outpatient visits that include an interview, saliva collection, lip biopsy, clinical laboratory studies, dry eye examination, and lip biopsy follow up, as needed. These are routine diagnostic procedures. Biopsy specimens may be used in clinical and laboratory studies, such as in vitro biochemical analysis or in vivo transplantation. Some of the Healthy Volunteers may be asked to participate in an MRI study of the salivary glands. * Objective: To obtain data from healthy volunteers for comparison with data from patients with salivary dysfunction. * Study population: Healthy volunteers aged 18-70 years old * Design: Observational * Outcome measures: Clinical and basic science data to serve as controls for comparisons with subjects presenting with salivary gland dysfunction Saliva is critical in maintaining oral health and comfort. Our laboratory has investigated several disorders of salivary glands. The purpose of this protocol is to obtain data from healthy volunteers for comparison with data from patients with salivary dysfunction. We plan to utilize the NIH Clinical Center Clinical Research Volunteer Program to solicit paid participation from healthy adults. Study procedures are accomplished in 2-3 outpatient visits that include an interview, saliva collection, lip biopsy, clinical laboratory studies, dry eye examination, and lip biopsy follow up, as needed. These are routine diagnostic procedures. Biopsy specimens may be used in clinical and laboratory studies, such as in vitro biochemical analysis or in vivo transplantation. Some of the Healthy Volunteers may be asked to participate in an MRI study of the salivary glands. The outcome measurement for this study is to determine those healthy subjects whose data and specimens can be used as control comparison for our patient subjects in our Sj(SqrRoot)(Delta)gren s syndrome studies (15-D-0051, 99-D-0070, 11-D-0094 and/or 11-D-0172).

Titre officielSalivary Evaluation in Healthy Volunteers 
Sponsor principalNational Institute of Dental and Craniofacial Research (NIDCR)
Dernière mise à jour : 24 septembre 2018
Issu d'une base de données validée par les autorités. Revendiquer cette étude

Protocole

Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.
Détails du design
173 participants à inclureNombre total de participants que l'essai clinique vise à recruter.

Éligibilité

Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.
Conditions
Critères
Tout sexeLe sexe biologique des participants éligibles à s'inscrire.
De 18 à 70 ansTranche d'âge des participants éligibles à participer.
Volontaires sains autorisésIndique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.
Conditions
Pathologie
Healthy
Salivary Gland Disease
Critères

* INCLUSION CRITERIA: * Healthy male or female volunteers from 18 to 70 years old. * Ability to understand and sign an informed consent document. EXCLUSION CRITERIA: * Known pregnancy. * Chronic medical illness, other than well-controlled hypertension or hyperlipidemia. * Chronic use of medications, with the exception of oral contraceptives, hormone replacement therapy, antihypertensives and antilipemics. * Have problems with dry mouth and/or dry eyes. * NIH employees who are subordinates/relatives/co-workers of investigators.



Centres d'étude

Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.
Cette étude comporte 1 site
Suspendu
National Institutes of Health Clinical Center, 9000 Rockville PikeBethesda, United StatesVoir le site

Terminé1 Centres d'Étude