Status:
RECRUITING
Anterior Cervical Discectomy and Fusion (ACDF) - Behavioral Intervention
Lead Sponsor:
NYU Langone Health
Conditions:
Dysphagia
Eligibility:
All Genders
21-99 years
Phase:
NA
Brief Summary
This study will prospectively recruit and enroll patients undergoing primary Anterior Cervical Discectomy and Fusion (ACDF) surgeries at NYU Langone. Participants will undergo pre-operative and six-we...
Eligibility Criteria
Inclusion
- Able and willing to sign consent form to participate in the study.
- Age between 21- 99 years.
- Scheduled to undergo ACDF surgery with surgeons in the departments of Neurosurgery or Orthopedic Surgery at NYU Langone.
Exclusion
- Patients with non-degenerative spine conditions, such as trauma, tumors, infection, radiation, and diabetes.
- Patients with prior posterior-approach cervical spine procedures.
- Patients undergoing ACDF revision procedures.
- Patients who report a pre-existing dysphagia as the result of a neurological deficit or disorder, head and neck cancer treatment, and/or muscular condition.
- Pregnancy. Female subjects must confirm they are not pregnant before enrolling in the study.
- Patients with chronic kidney disease, limiting their ability to consume high levels of protein.
- Patients with known allergies to ingredients listed in Premier Protein Clear drinks.
Key Trial Info
Start Date :
October 15 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2025
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT06520579
Start Date
October 15 2024
End Date
September 1 2025
Last Update
April 15 2025
Active Locations (1)
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1
NYU Langone Health
New York, New York, United States, 10016