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NCT05886738
Investigating the Effect of Short-term Fasting on T Cell Metabolism, Function, and Phenotype in Obesity
NA trial testing Fasting in Obesity in 20 participants. Status unknown.
30 August 2023
Quick facts
| Lead sponsor | University of British Columbia |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | basic science |
| Enrollment | 20 |
| Start date | 1 June 2023 |
| Primary completion | 30 August 2023 |
| Estimated completion | 30 August 2023 |
Drugs / interventions tested
- Fasting
Conditions studied
- Obesity — all drugs for Obesity →
- Fasting — all drugs for Fasting →
- T-Cell Dysfunction — all drugs for T-Cell Dysfunction →
Sponsor
University of British Columbia
Who can join
Adults 19 to 69, any sex, with Obesity or Fasting. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The immune system is made up of many types of immune cells, each of which play a specialized role in protecting against pathogens. T cells are a crucial part of the adaptive immune system, and receive signals from the body's metabolism which tell them whether they should become activated to respond to an infection or if they should stay in their resting state. In obesity, the body's metabolism shifts and these T cells become less effective at protecting against infection and instead start to increase inflammation which is involved in obesity-related health conditions. The investigators are conducting this study because the investigators are interested in understanding how fasting, which will alter the metabolic signals that T cells receive, might impact the types of T cells that are present and how they respond to activating signals. Additionally, the investigators are interested in understanding if these responses differ between T cells from individuals with obesity versus lean individuals.
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
-
Reversible histone deacetylase activity catalyzes lysine acylation.
Tsusaka T, Najar MA, Schwarz B, Bohrnsen E, et al · · 2025 · cited 15× · PMID 40140626 · DOI 10.1038/s41589-025-01869-5 -
Altered immunometabolic response to fasting in humans living with obesity.
Neudorf H, Sandilands RE, Ursel S, Shaba H, et al · · 2025 · cited 2× · PMID 40662191 · DOI 10.1016/j.isci.2025.112872 -
Metabolic responses to 48 h fasting and refeeding in adults with and without obesity.
Sandilands R, Neudorf H, Ursel S, Shaba H, et al · · 2026 · PMID 41650389 · DOI 10.1139/apnm-2025-0447
Verify or expand the search:
- PubMed search for NCT05886738
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT05886738 (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 University of British Columbia
- Last refreshed: 2 June 2023
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/NCT05886738.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing