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NCT05336032
Ethnic Variability in Glycemic and Hunger Satiety Response to Rice in Overweight Adults
NA trial testing Food (rice) in Glycemic Response in 20 participants. Status unknown.
30 August 2022
Quick facts
| Lead sponsor | Rashid Centre for Diabetes and Research |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | single |
| Primary purpose | diagnostic |
| Enrollment | 20 |
| Start date | 1 April 2022 |
| Primary completion | 30 August 2022 |
| Estimated completion | 30 October 2022 |
| Sites | 1 location across United Arab Emirates |
Drugs / interventions tested
- Food (rice)
Conditions studied
- Glycemic Response — all drugs for Glycemic Response →
Sponsor
Rashid Centre for Diabetes and Research
Who can join
Adults 18 to 55, any sex, with Glycemic Response. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Evidence has./ indicated increased risk of type 2 diabetes with white rice consumption in Asian population. It is shown that glycemic response to carbohydrate-containing food may differ in people of different ethnicities. The large increment in glucose concentration induced by high glycemic index food often exaggerates the body's anabolic responses, which facilitates the overproduction of insulin and eventually results in pancreatic beta-cell failure, causing type 2 diabetes mellitus. Given that rice is the staple food of Asians and Emiratis, and extent to which rice influences postprandial glycemia could have potential relevance in the prevention and treatment of diabetes. In this study, the investigators intend to compare the glycemic and hunger satiety response to rice among overweight Emiratis, Asians, and Caucasian. The primary objective of the study is to compare the glycemic (glucose) and hunger satiety (hormone ghrelin and peptide YY) response to glucose and rice among overweight Emiratis, Asians, and Caucasians.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Ethnic Variability in Glucose and Insulin Response to Rice Among Healthy Overweight Adults: A Randomized Cross-Over Study.
Sadiya A, Jakapure V, Kumar V. · · 2023 · cited 6× · PMID 37063254 · DOI 10.2147/dmso.s404212
Verify or expand the search:
- PubMed search for NCT05336032
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Glycemic Response
Currently open trials in the same condition.
- NCT04881019 — PRediction Of Glycemic RESponse Study · active not recruiting
Other Rashid Centre for Diabetes and Research trials
Trials by the same sponsor.
- NCT04273412 — Lifestyle Intervention for Prevention of Gestational Diabetes Mellitus in the UAE Population · NA · completed
- NCT03388229 — Association Between Dietary Pattern and Glycemic Control Among Type 2 Diabetes Patients in the Unites Arab Emirates · completed
- NCT03644134 — A Personalized Intervention to Manage Physiological Stress and Improve Sleep Patterns · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05336032 (US National Library of Medicine, public domain)
- 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 Rashid Centre for Diabetes and Research
- Last refreshed: 26 October 2022
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/NCT05336032.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing