Skip to content

A trial to evaluate the effects of a D-xylose preload, with or without sitagliptin, on incretin hormone secretion, gastric emptying, and postprandial glycaemia in patients with type 2 diabetes mellitus.

A randomised placebo controlled crossover trial to evaluate the effects of a D-xylose preload, with or without sitagliptin, on incretin hormone secretion, gastric emptying, and postprandial glycaemia in patients with type 2 diabetes mellitus.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612001131842
Enrollment
12
Registered
2012-10-23
Start date
2011-11-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The study will evaluate the effects of a D-xylose preload, with or without sitagliptin, on incretin hormone secretion, gastric emptying, and postprandial glycaemia in patients with type 2 diabetes.

Interventions

Each subject will undergo four study visits, in which they will receive a sweet "preload" drink, containing either 50g D-xylose or 80mg sucralose (negative control), after receiving either 100mg sitagliptin or placebo. The four studies will occur in double-blind, randomised fashion, separated by 3 days. Sitagliptin or placebo tablets will be taken at 2200 the evening before each study, and the sweet preload will be consumed the following morning, between T=-40 to -38 min, before a mashed potato

Each subject will undergo four study visits, in which they will receive a sweet "preload" drink, containing either 50g D-xylose or 80mg sucralose (negative control), after receiving either 100mg sitagliptin or placebo. The four studies will occur in double-blind, randomised fashion, separated by 3 days. Sitagliptin or placebo tablets will be taken at 2200 the evening before each study, and the sweet preload will be consumed the following morning, between T=-40 to -38 min, before a mashed potato meal (65g powdered potato and 20g glucose reconstituted with 200mL water and one egg yolk containing 13C octanoic acid) consumed between T=0 to 5 min.

Sponsors

Royal Adelaide Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
20 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

Patients with type 2 diabetes mellitus

Exclusion criteria

Medications affecting gut function; Alcohol intake >20g daily or cigarette smoking; Significant gastrointestinal disease or surgery; Impaired liver or renal function; Blood donation within 3 months

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026