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A prospective cohort study of taste changes due to weight loss in highly obese patients

Not Applicable
Conditions
Obesity
Registration Number
JPRN-UMIN000045074
Lead Sponsor
Wakayama Medical University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
26
Inclusion Criteria

Not provided

Exclusion Criteria

1. Patients with a history of severe ketosis or diabetic coma within 6 weeks of the start of the study 2. Patients who develop severe hypoglycemia within 6 weeks of the start of the study 3. Patients with severe renal dysfunction (eGFR <15 mL / min / 1.73 m2) or patients with end-stage renal disease on dialysis 4. Patients with proliferative retinopathy (excluding patients who have undergone photocoagulation and have stable state) 5. Patients with severe gastrointestinal disorders within 2 weeks of the study 6. Pregnant or potentially pregnant women and lactating patients 7. Patients with severe infections and serious trauma 8. Patients with other serious food allergies, including dairy products 9. Other patients who the principal investigator deems inappropriate as subjects

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Taste rank
Secondary Outcome Measures
NameTimeMethod
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