Viewing Study NCT06522958



Ignite Creation Date: 2024-10-26 @ 3:36 PM
Last Modification Date: 2024-10-26 @ 3:36 PM
Study NCT ID: NCT06522958
Status: ENROLLING_BY_INVITATION
Last Update Posted: None
First Post: 2024-07-23

Brief Title: Effect of Novel High Dissolving Transitional Foods
Sponsor: None
Organization: None

Study Overview

Official Title: Comparative Study of the Effects of Novel High Dissolving Transitional Foods on Post-Operative Outcomes for Patients Undergoing Craniofacial Surgery
Status: ENROLLING_BY_INVITATION
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None