Adults 18 to 65, any sex, with Healthy Obesity, Metabolically or Appetite Regulation. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Change in Weight Loss Compared to BaselinePrimary· Baseline and 12 weeks
The weight assessed by a body scale
Group
Value
95% CI
Experimental Group
-2.6
± 0.9
Inulin
-3
± 1.04
Glucose Blood Level Baseline to 12 WeeksSecondary· Baseline, 12 weeks
Baseline
Group
Value
95% CI
Experimental Group
4.9
± 0.1
Inulin
4.4
± 0.1
12 weeks
Group
Value
95% CI
Experimental Group
5.1
± 0.1
Inulin
4.8
± 0.1
Insulin Level in SerumSecondary· Baseline, 12 weeks
Baseline
Group
Value
95% CI
Experimental Group
50.4
± 10.8
Inulin
48.9
± 18.3
12 weeks
Group
Value
95% CI
Experimental Group
41.0
± 6.7
Inulin
46.0
± 21.1
Sponsor's own description
The current protocol aims to investigate the impact of the propionate ester in conjugation with restricted diet on appetite and weight loss.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
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Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Imperial College London
Last refreshed: 20 November 2019
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03322514.