A study on changes in nutritional status in patients with medication-related osteonecrosis of the jaw
- Conditions
- Medication-related osteonecrosis of the jaw
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Patients aged 18 years or older at the time of informed consent Regardless of gender Performance Status From 0 to 2 Patients who have given written informed consent of their own free will after receiving sufficient explanation about participating in this study
Patients who have difficulty in taking nutritional supplements orally before surgery
For example, patients with severe dementia or on parenteral nutrition
Patients on dialysis
Patients with diabetes (HbA1c of 6.5 or high)
Obese patients (BMI of 25 or high)
Patients with milk allergy or soy allergy
Other patients who are judged by the attending physician to be inappropriate as research subjects
Study & Design
- Study Type
- Interventional
- Study Design
- single assignment
- Primary Outcome Measures
Name Time Method - Nutritional status 8 days after surgery (serum albumin, ser um total protein, prealbumin)
- Secondary Outcome Measures
Name Time Method Postoperative complications Presence or absence of postoperative complications
Nutritional status changes 1 to 3 months after surgery Changes in nutritional status (weight change rate, BMI, CONUT value)