Accepts Healthy Volunteers
Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms
An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.
An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.
Searching Both is inclusive of interventional and observational studies.
|Observational [Patient Registry]|
|Eligible Ages||7 Years - 18 Years|
- - Schoolchildren from various districts of Moscow selected as a result of questioning in the risk group for the development of celiac disease - Availability of written informed consent of the child over 14 years of age to participate in the study; - Availability of written informed consent of the parent of the child to participate in the study; - Age from 7 to 18 years; - Male and female gender; - The number of points according to the results of the survey is more than 25.
- - Age up to 7 years and over 18 years.
This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.
Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.
Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.
Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.
Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.
The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.
|I.M. Sechenov First Moscow State Medical University|
The person who is responsible for the scientific and technical direction of the entire clinical study.
|Svetlana Erdes, Ph.D|
|Principal Investigator Affiliation||Sechenov First Moscow State Medical University|
Category of organization(s) involved as sponsor (and collaborator) supporting the trial.
The disease, disorder, syndrome, illness, or injury that is being studied.
|Celiac Disease in Children|
The purpose of this screening program is to identify people at high risk for developing celiac disease, which is due to the genetic intolerance of gluten
- - a protein found in wheat, rye and barley.
Contact a Trial Team
If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.