4618432
Last Update Posted: 2023-06-13
Recruiting has ended
All Genders accepted | 2 Years + |
26 Estimated Participants | No Expanded Access |
Observational Study | Does not accept healthy volunteers |
Collection of Clinical Data and Specimens for Research on Head and Neck and Communication Disorders
Study Description:
It may be in the interest of the NIDCD Clinical Research Program (CRP) to collect clinical data or specimens generated in the diagnosis and treatment of head and neck or communication disorders and to evaluate patients to determine candidacy for intramural clinical studies. This protocol will provide the administrative vehicle to enable the evaluation and provision of clinical care for patients with head and neck and communication disorders by the NIDCD CRP, Clinical Center, and consult services. No investigational therapies will be administered in this
study.
Objectives and Endpoints:
(Summation)To collect clinical data or specimens generated in the diagnosis and treatment of head and neck or communication disorders
(Summation)To evaluate patients to determine candidacy for intramural clinical studies
Study Population:
Patients at risk, suspected of having, have a history of, or currently have a diagnosed head and neck or communication disorder referred to NIDCD Clinical Investigators by the Intramural Consult Service or community providers
Description of Sites:
NIH Clinical Center
Study Duration:
10 years
Study Description:
It may be in the interest of the NIDCD Clinical Research Program (CRP) to collect clinical data or specimens generated in the diagnosis and treatment of head and neck or communication disorders and to evaluate patients to determine candidacy for intramural clinical studies. This protocol will provide the administrative vehicle to enable the evaluation and provision of clinical care for patients with head and neck and communication disorders by the NIDCD CRP, Clinical Center, and consult services. No investigational therapies will be administered in this
study.
Objectives and Endpoints:
(Summation)To collect clinical data or specimens generated in the diagnosis and treatment of head and neck or communication disorders
(Summation)To evaluate patients to determine candidacy for intramural clinical studies
Study Population:
Patients at risk, suspected of having, have a history of, or currently have a diagnosed head and neck or communication disorder referred to NIDCD Clinical Investigators by the Intramural Consult Service or community providers
Description of Sites:
NIH Clinical Center
Study Duration:
10 years
Eligibility
Relevant conditions:
Head and Neck Carcinoma
If you aren't sure if you meet the criteria above speak to your healthcare professional. Criteria may be updated but not reflected here, do not hesitate to contact the trial if you think are close to fitting criteria.
Inclusion criteria
Exclusion criteria
locations
Data sourced from ClinicalTrials.gov