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Evaluating the Safety and Efficacy of a Probiotic on IBS Symptom Severity in Adults With Diarrhoea-predominant Irritable Bowel Syndrome

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT05754177
Title field or adapter rule
{'original_value': 'Evaluating the Safety and Efficacy of a Probiotic on IBS Symptom Severity in Adults With Diarrhoea-predominant Irritable Bowel Syndrome', 'source_field': 'protocolSection.identificationModule.officialTitle'}
Ingested At
2026-10-31T23:27:35.680857+00:00
Published At
2025-03-06T00:00:00+00:00
Record Updated At
2025-03-06
Source Retrieved At
2026-10-31T22:18:52.668840+00:00
Timestamp Basis
ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter
Date limitation
ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Irritable Bowel Syndrome With Diarrhea", "Irritable Bowel Syndrome"]
protocolSection.statusModule.lastUpdatePostDateStruct
{"date": "2025-03-06", "type": "ACTUAL"}
protocolSection.identificationModule.nctId
"NCT05754177"
protocolSection.identificationModule.officialTitle
"Evaluating the Safety and Efficacy of a Probiotic on IBS Symptom Severity in Adults With Diarrhoea-predominant Irritable Bowel Syndrome"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["NA"]
protocolSection.statusModule.resultsFirstPostDateStruct
null

Study condition terms

  • Irritable Bowel Syndrome With Diarrhea (protocolSection.conditionsModule.conditions)
  • Irritable Bowel Syndrome (protocolSection.conditionsModule.conditions)

Interventions recorded in this study

  • {'armGroupLabels': ['Probiotic'], 'description': 'Participants in this arm will receive a daily dose of 1x10\\^10 Colony Forming Unit (CFU) of a single strain probiotic (live bacteria), administered orally by 1 capsule a day, for 84 days', 'name': 'Probiotic', 'type': 'DIETARY_SUPPLEMENT'} (protocolSection.armsInterventionsModule.interventions[])
  • {'armGroupLabels': ['Placebo'], 'description': 'Participants in this arm will receive an equivalent placebo for 84 days.', 'name': 'Placebo', 'type': 'OTHER'} (protocolSection.armsInterventionsModule.interventions[])

An intervention appearing in a study record does not establish an effect or an approved use.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.