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NCT05086458

Impact of Probiotics Supplement on the Gut Microbiota in Caesarean-born Infants

Status unknown NA Last updated 21 October 2021
What this trial tests

NA trial testing probiotics in Gut Microbiota in 30 participants. Status unknown.

Timeline
17 August 2021
Primary endpoint
17 October 2021
17 October 2021

Quick facts

Lead sponsorShanghai 10th People's Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment30
Start date17 August 2021
Primary completion17 October 2021
Estimated completion17 October 2021
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai 10th People's Hospital

Who can join

Adults 1 Hour to 42 Days, any sex, with Gut Microbiota. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the effect of probiotics on the gut microbiota of infants born by cesarean section.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Effect of Probiotic Supplementation on the Gut Microbiota Composition of Infants Delivered by Cesarean Section: An Exploratory, Randomized, Open-label, Parallel-controlled Trial.
    Gong Y, Zhong H, Wang J, Wang X, et al · · 2023 · cited 4× · PMID 37712964 · DOI 10.1007/s00284-023-03444-4

Verify or expand the search:

Other trials of probiotics

Trials testing the same drug.

Other recruiting trials for Gut Microbiota

Currently open trials in the same condition.

Other Shanghai 10th People's Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT05086458.

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