Improving Nutritional Status With Oral Nutritional Supplement in Chinese Elderly

Malnutrition Clinical Trial

Official title:

Improving Nutritional Status With Oral Nutritional Supplement in Chinese Elderly

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT02360722
• Other study ID #: BL26
• Status: Withdrawn
• Phase: Phase 4
• First received: January 27, 2015
• Last updated: November 30, 2016
• Start date: October 2016
• Est. completion date: December 2017

Study information

• Verified date: November 2016
• Source: Abbott Nutrition
• Contact: n/a
• Is FDA regulated: No
• Health authority: China: Ethics Committee
• Study type: Interventional

Clinical Trial Summary

This is a single- country, interventional, double-arm study involving Chinese Elderly subjects.

Description:

This study aims to understand the following:

1. The effect of long-term Oral Nutritional Supplementation (ONS) on improving nutritional and health status in Chinese elderly.

2. The impact of long-term ONS on health cost including both medical cost and social health care burdens.

3. The impact of long-term ONS on life quality of the elderly. The study includes Screening Visit (Day -7~0), and Visit 1(Day 0) to Visit 7 (Day 168±3). Enrollment of anticipated 666 subjects, Male or female Chinese ages >= 60 years, to get 400 evaluable subjects.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: December 2017
• Est. primary completion date: July 2017
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 60 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Male or female Chinese ages >= 60 years.

2. Subject is ambulatory.

3. Subject with risks of malnutrition defined as DETERMINE score >=3

4. Subject's BMI is below 28.

5. Subject has experienced hospital stay or surgery within 6 months prior to enrollment;

6. Subject if takes any medications for concomitant chronic diseases should be in stable dosage for at least 3 weeks.

7. Subject plans to live in the community for more than 6 months after recruitment.

8. Subject has voluntarily signed and dated an informed consent form, approved by an Independent Ethics Committee/Institutional Review Board (IEC/IRB) prior to any participation in the study.

Exclusion Criteria:

1. Subject has history of allergy to any ingredient in the study product

2. Subject dislikes the experimental product

3. Subject has been diagnosed with diabetes.

4. Subject who has malignancy expected to receive chemotherapy/ radiotherapy scheduled during the study period,

5. Subject has a life expectancy less than 6 months.

6. Subject who has reported chronic liver disease or liver cirrhosis or liver failure or any liver diseases not suitable for the study as the study physician's opinion.

7. Subject who has reported impacted renal function as eGFR < 30 mL/min/1.73 m2 or renal dysfunction severe greater than stage 4 or any other renal diseases not suitable for the study as the study physician' s opinion.

8. Subject who has experienced fever or diarrhea within one week prior to enrollment.

9. Subject who is expected to have scheduled major surgery during the study period.

10. Subject who has physical disabilities such as loss of hand or foot or limbs or any other physical disability which may affect the muscle mass measurement by the opinion of the study physician.

11. Subject has an implanted electronic device or orthopedic metal implantations, such as pacemaker, cardiac defibrillator, subcutaneous injection pump, or metal hip, metal knee joint, metal fracture internal fixation, etc.

12. Subject who has active tuberculosis (TB), hepatitis, or HIV infection as self-reported at enrollment.

13. Subject has severe dementia or delirium, brain metastases, eating disorder, history of significant neurological or psychiatric disorder, or other conditions that may interfere with study product consumption or compliance with study protocol procedures in the opinion of the principal investigator or study physician.

14. Subject is drug addicted or alcohol addicted

15. Subject has any other disease or situation who should not to participate in the study by the opinion of study physicians.

16. Subject is participating in other clinical trials which are not approved by AN

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

• Malnutrition

Intervention

Other:
• Oral Nutritional Supplement
Will receive ONS twice a day for 6 months and two nutritional education at baseline and 3 months after intervention
• Nutritional Education
Two nutritional education courses at baseline and 3 months after intervention

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Abbott Nutrition

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change of body weight from baseline to the end of the study		24 weeks	No
Secondary	Total number of sick days due to Upper Respiratory Tract Infections (URTI)		24 weeks	No