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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05612048
Other study ID # 22-370
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 3, 2022
Est. completion date November 2025

Study information

Verified date April 2024
Source Memorial Sloan Kettering Cancer Center
Contact Steven Maron, MD
Phone 646-888-6780
Email marons@mskcc.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The researchers are doing this study to find out more about what may lead to the loss of tooth enamel (the thin outer covering of the tooth) and how often it happens in people with esophagogastric cancer, colorectal cancer, pancreatic cancer, breast cancer, head and neck cancer, or non-small cell lung cancer, or a healthy volunteer.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date November 2025
Est. primary completion date November 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Subject is willing and able to provide written informed consent. - Patients with a history of esophagogastric, HNSCC, PDAC, CRC, or NSCLC or healthy controls - Patients must be able to fully comprehend and complete the survey and be willing to have pictures taken of their teeth with a camera or intra-oral camera. - Patients must be able to understand English language or have access to adequate translation services. - Age = 18 years old. Exclusion Criteria: - Subjects without evaluable molars or with significant molar dental work precluding dentists from assessing enamel status, Note: evaluable is defined as having bilateral assessable mandibular molars, or erosions present in the remaining assessable quadrants. - For healthy controls only, patients cannot have a non-skin cancer history nor presenting for a procedure evaluating reflux symptoms.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Survey
This is a 15-item questionnaire. The questionnaire asks subjects to quantify, during a specified duration of time, the number of times they have consumed or completed a task (ex. alcohol intake, cigarette use, and teeth brushing frequency). Additionally, the questionnaire further asks subjects to quantify their GERD symptoms and risk factors prior to diagnosis. All study procedures will be completed in one visit as part of a standard-of-care clinic visit.
Intra-oral camera
Intraoral pictures of molars and incisors in 13 key regions
Optional Salvia sample
Cohort 1 only. Participant is responsible for collecting and bringing the salvia sample to clinic.

Locations

Country Name City State
United States Memorial Sloan Kettering Cancer Center (All Protocol Activities) New York New York

Sponsors (1)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The incidence of dental erosions scored with a modified BEWE index. 1 year
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