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Gastric Emptying Study After Administration of a High Caloric Sip Feed

NCT00600678 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2008-05-15

No results posted yet for this study

Summary

Measurement of gastric emptying time of an oral nutritional supplement (ProvideXtra DRINK) by using the paracetamol absorption method in healthy volunteers.

Conditions

  • Enteral Nutrition

Interventions

DIETARY_SUPPLEMENT

ProvideXtra DRINK (oral nutritional supplement, food for special medical purposes)

Single, oral administration of nutritional supplement under fasting condition within 2 minutes.

Sponsors & Collaborators

  • Fresenius Kabi

    lead INDUSTRY

Principal Investigators

  • Frank Donath, MD · SocraTec R&D GmbH, Clinical Pharmacology Unit, Erfurt, Germany

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-11-30
Primary Completion
2007-12-31
Completion
2008-01-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00600678 on ClinicalTrials.gov