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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02698540
Other study ID # DA13
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 28, 2016
Est. completion date May 2018

Study information

Verified date August 2018
Source Abbott Nutrition
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose is to observe the compliance to a high-calorie, high protein peptide-based nutritional supplement after 3 months in a malnourished population with impaired gastrointestinal tolerance living in nursing homes and as outpatients.


Recruitment information / eligibility

Status Completed
Enrollment 95
Est. completion date May 2018
Est. primary completion date May 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Subject is considered malnourished, or is at risk for malnutrition based on MUST score =2.

- Subject is =18 years old.

- Subject has a condition that would benefit from a high calorie, higher protein ONS for GI tolerance impairment (e.g., diarrhea, nausea, vomiting, satiety or bloating).

- Subject conforms to the requirements set forth on the study product label.

- Subject is under the care of a health care professional for malnutrition and has recently (within the last 7 days prior to participating in this study) been prescribed 2 servings/day of the study ONS. Subject must have been naïve to ONS for GI tolerance impairment prior to being prescribed the study ONS.

Exclusion Criteria:

- The study physician determines the subject is not fit to participate

- Subject cannot provide informed consent to participate in the study.

- Subject cannot safely consume the oral nutritional supplement.

- Renal or liver failure (GFR< 60 ml/min or AST/ALTx3 normal) upper limit.

- Type 1 or type 2 diabetes.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Nutritional Supplement
High calorie, high protein peptide based

Locations

Country Name City State
Spain Hospital Universitario Germans Trias i Pujol Badalona
Spain Hospital de Cruces 1758 Barakaldo
Spain Hospital de Cruces 2029 Barakaldo
Spain Hospital de Jerez Cadiz
Spain Hospital Universitario Reina Sofía de Córdoba Córdoba
Spain Hospital Universitario Campus de la Salud Granada
Spain Complejo Asistencial Universitario de Leon, Endocrinologia y Nutricion Leon
Spain Hospital Ramón y Cajal Madrid
Spain Hospital Universitario de Móstoles Madrid
Spain Hospital Universitario La Paz Madrid
Spain Hospital Universitario Principe de Asturias Madrid
Spain Centro Médico San Juan de la Cruz Málaga
Spain Hospital Costa del Sol 1740 Marbella
Spain Hospital Costa del Sol 1743 Marbella
Spain Hospital Rey Juan Carlos Móstoles
Spain Hospital General Universitario Reina Sofía de Murcia Murcia
Spain Hospital Vega Baja Orihuela
Spain Hospital del Bierzo Ponferrada
Spain Hospital Universitario Virgen del Rocío Sevilla
Spain Hospital Clínico Universitario de Valencia 1695 Valencia
Spain Hospital La Ribera Valencia
Spain Hospital de Vic Vic
Spain Hospital Universitario Miguel Servet Zaragoza

Sponsors (1)

Lead Sponsor Collaborator
Abbott Nutrition

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Study Product Compliance Subject reported diaries Baseline to Week 12
Secondary Body Weight Baseline to Week 12
Secondary Nutrition Status Healthcare Professional completed screening Baseline to Week 12
Secondary Quality of Life Subject reported questionnaire Baseline to Week 12
Secondary Gastrointestinal Tolerance Subject reported scale Baseline to Week 12
Secondary Body Mass Index Baseline to Week 12
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