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.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Caregiver-Reported Rating of Feeding Experience
Timeframe: Week 1 Post-Operation (Post-Op)
Caregiver-Reported Rating of Feeding Experience
Timeframe: Week 3 Post-Op