Enhanced Recovery After Surgery (ERAS): Pilot Study of Carbohydrate (CHO) Loading Prior to Head and Neck Cancer Surgery
Not Applicable
- Conditions
- head and neck cancerCancer - Head and neck
- Registration Number
- ACTRN12618000218291
- Lead Sponsor
- Sydney Local Health District
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Adult patients >18 years undergoing major surgery with free flap reconstruction for head and neck cancer
- Able to speak adequate English to understand patient information sheet and give informed consent
- Willingness to participate in the proposed research
Exclusion Criteria
- Patients at high risk of refeeding syndrome as determined by pre-admission clinic dietitian assessment visit
- Patients with dysphagia requiring thickened fluids
- Patients with diabetes requiring insulin
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome of the study is the safety and tolerability of pre-operative CHO loading. <br>Tolerability will be determined by a visual analogue scale whereby patient-reported wellbeing measures eg thirst, hunger, anxiety, nausea, fatigue, pain etc will be captured.<br>Safety will be determined by presence/absence of adverse events. Every endeavour will be made through careful selection of eligibility/ineligibility criteria, potential adverse events may be nausea, vomiting, aspiration and hyperglycaemia which will be captured.[Day of Surgery -1, Days 1, 7, 28 Post-op, on Discharge, ]
- Secondary Outcome Measures
Name Time Method