Blood Glucose Response After Oral Intake of Lactulose in Healthy Volunteers

NACompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

November 30, 2016

Primary Completion Date

February 28, 2017

Study Completion Date

February 28, 2017

Conditions
Blood Glucose
Interventions
DIETARY_SUPPLEMENT

Lactulose crystals 10 g

White or almost white crystalline powder used as food ingredient. The products will be provided in sachets to be dissolved in 250 mL water.

DIETARY_SUPPLEMENT

Lactulose crystals 20 g

White or almost white crystalline powder used as food ingredient. The products will be provided in sachets to be dissolved in 250 mL water.

DIETARY_SUPPLEMENT

Lactulose liquid 10 g

Clear, viscous liquid, colourless or pale brownish-yellow liquid syrup (solution). The products will be provided in sachets to be dissolved in 250 mL water.

DIETARY_SUPPLEMENT

Lactulose liquid 20 g

Clear, viscous liquid, colourless or pale brownish-yellow liquid syrup (solution). The products will be provided in sachets to be dissolved in 250 mL water.

DIETARY_SUPPLEMENT

Oral glucose 20 g

White crystalline powder used as food ingredient. To standardise for 20 g glucose, 22 g glucose monohydrate will be used. The products will be provided in sachets to be dissolved in 250 mL water.

DIETARY_SUPPLEMENT

Still water

Still water will be used. Water from the same source will be also used to dissolve investigational and control products.

Trial Locations (1)

73728

CRO BioTeSys GmbH, Esslingen am Neckar

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Fresenius Kabi

INDUSTRY

NCT02968498 - Blood Glucose Response After Oral Intake of Lactulose in Healthy Volunteers | Biotech Hunter | Biotech Hunter