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NCT03994276
The Postprandial Effects of Chick-Pea Consumption on Glucose, Insulin, and Gut Hormone Responses (PEA-POD).
NA trial testing Chickpea powder in Postprandial Period in 29 participants. Completed in 20 May 2020.
10 February 2020
Quick facts
| Lead sponsor | King's College London |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | double |
| Primary purpose | prevention |
| Enrollment | 29 |
| Start date | 25 June 2019 |
| Primary completion | 10 February 2020 |
| Estimated completion | 20 May 2020 |
| Sites | 1 location across United Kingdom |
Drugs / interventions tested
- Chickpea powder
Conditions studied
- Postprandial Period — all drugs for Postprandial Period →
Sponsor
King's College London
Who can join
Adults 18 to 45, any sex, with Postprandial Period. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Pulses have a high fibre content, contribute to lowering fasting blood cholesterol levels and improving glycaemic control, and have shown also considerable promise in supporting the dietary management of cardiovascular disease (CVD), type-2 diabetes mellitus (T2DM) and obesity. It is now established that cellular integrity (maintenance of cell wall structure) is a key factor responsible for the low glycaemic index (GI) of pulses. The maintenance of the cell wall structure restricts starch digestion and therefore glucose production in the gut. Thus, cell damage results in a loss of such properties and also the potential health benefits to consumers. This knowledge has presented an opportunity to exploit alternative processing techniques for the manufacture of pulse-based ingredients. We have successfully created a dry powder consisting predominantly of intact cells which still retains low digestibility (\>60% resistant starch). This chickpea powder (CPP) was found to be stable under long-term storage, has a neutral taste and aroma, and showed promise as a low GI 'flour-substitute'. This study will investigate blood sugar, insulin and gut hormone levels (post-prandial glycaemic, insulinaemic and hormone responses) following the consumption of CPP consumed at breakfast, as a drink and incorporated into a food matrix (bread).
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
The impact of replacing wheat flour with cellular legume powder on starch bioaccessibility, glycaemic response and bread roll quality: A double-blind randomised controlled trial in healthy participants.
Bajka BH, Pinto AM, Ahn-Jarvis J, Ryden P, et al · · 2021 · cited 31× · PMID 33941996 · DOI 10.1016/j.foodhyd.2020.106565 -
Enhanced secretion of satiety-promoting gut hormones in healthy humans after consumption of white bread enriched with cellular chickpea flour: A randomized crossover study.
Bajka BH, Pinto AM, Perez-Moral N, Saha S, et al · · 2023 · cited 23× · PMID 36811474 · DOI 10.1016/j.ajcnut.2022.12.008
Verify or expand the search:
- PubMed search for NCT03994276
- Europe PMC full search
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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 NCT03994276 (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 King's College London
- Last refreshed: 2 September 2020
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/NCT03994276.
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