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ENROLLING BY INVITATION
NCT06522958
NA

Effect of Novel High Dissolving Transitional Foods

Sponsor: NYU Langone Health

View on ClinicalTrials.gov

Summary

This is a prospective comparative study, where patients who meet inclusion criteria undergoing a craniofacial procedure will either be provided with novel high dissolving transitional foods for use in the post-operative period (Intervention Group) or will not be provided the food and will proceed as per current standard of care (Standard of Care Group). Both groups will be followed pre-operatively at time of pre-operative visit, and will be followed in the post-operative period, with two visits at 1 and 3 weeks post-operatively, respectively.

Official title: Comparative Study of the Effects of Novel High Dissolving Transitional Foods on Post-Operative Outcomes for Patients Undergoing Craniofacial Surgery

Key Details

Gender

All

Age Range

6 Months - 18 Years

Study Type

INTERVENTIONAL

Enrollment

160

Start Date

2024-08-09

Completion Date

2027-08

Last Updated

2025-06-25

Healthy Volunteers

No

Interventions

DIETARY_SUPPLEMENT

High Dissolving Transitional Food

Transitional foods are solid foods that rapidly change texture in the presence of moisture (e.g., water or saliva) or temperature change. Duration of consumption of the investigational agent will include the time of the surgery until the second post-operative evaluation. This is estimated to be approximately 1-2 months in total.

Locations (1)

NYU Langone Health

New York, New York, United States