Patients undergoing oral surgery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients aged 20 years or older at the date of informed consent 2) Patients who plan to receive an oral surgery 3) Patients who are indicated to receive the trans-nasal nutrition as the postsurgical nutrition management 4) Patients who provide voluntary consent after receiving a sufficient oral and written explanation about the study
Exclusion criteria
Exclusion criteria: 1) Patients who take or receive the drugs prohibited to use during the study period 2) Patients who have the disease history of gastroduodenal ulcer or other upper gastrointestinal diseases 3) Patients who might have food allergies or allergies to the products used in the study 4) Patients who receive anticancer drugs or radiotherapy 5) Patients who deemed to be unsuitable for inclusion in the study due to concomitant diseases including hepatic disorder, renal disorder, and cardiac disorder 6) Female patients who are pregnant, lactating, or potentially pregnant 7) Others who are deemed unsuitable for inclusion in the study for any other reason based on decision by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| An achievement rate of nutritional control When all the following conditions are met, the nutritional control is defined to be "achieved." - Ninety percent or more of the targeted amount of test diet was administered. - The number of use of antiflatulents is two or smaller. - The frequency of stool per day is three times or lower. - Neither watery stool nor muddy stool was observed. | — |
Secondary
| Measure | Time frame |
|---|---|
| - Nutritional parameters (blood albumin, blood total protein, body weight) | — |
Countries
Japan
Contacts
Tokyo medical and dental university (gudaduate school) maxillofacial surgery