Understanding the Burden of ACC Through the Eyes of Patients
Completed
Conditions studied: Adenoid Cystic Carcinoma
In brief
This is a comprehensive, cross-sectional study conducted with approximately 40-60 individuals affected by ACC who may know the results of molecular profiling of their tumor. Primary Objectives: * To identify the specific burdens faced by patients with ACC * To compare/contrast the burdens faced by patients with ACC at different disease stages (no evident disease, metastatic disease/watchful waiting, progressive disease)
Key facts
- Study ID
- NCT04706845
- Run by
- Ayala Pharmaceuticals, Inc,
- People needed
- 46
- Starts
- 2021-01-11
- Expected to finish
- 2023-08-16
- Last updated by the study team
- 2023-09-29
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Participant must be a person diagnosed with ACC who is 18 years or older
- For patients with metastatic disease; watchful waiting or progressive disease, participants must know the results of molecular profiling of their tumor
- Histologically-confirmed diagnosis of ACC with written proof of disease and molecular profile of tumor provided. This can be a note showing genetic diagnosis from a relevant testing laboratory, physician consult notes, a medical record of diagnosis, or any other single piece of documentation that connects your name/the patient's name with ACC.
- Able to read, write and understand English, Hebrew, Arabic, or Russian
- Able to grant informed consent
- Willing to participate in a 45-to-60-minute telephone interview, including follow up questions (if necessary)
You may not qualify if…
- Inability to meet any of the inclusion criteria
Where it is running
- Engage Health — Eagan, Minnesota, United States
Full record on ClinicalTrials.gov
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