CLINICAL_TRIALS ClinicalTrials.gov record update

Efficacy of Repeated Transcranial Magnetic Stimulation Combined With a Live Probiotic Tablet (Combined Bifidobacterium, Lactobacillus, Enterococcus and Bacillus Cereus Tablets, Live) in Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D)

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT06960369
Title field or adapter rule: {'original_value': 'Efficacy of Repeated Transcranial Magnetic Stimulation Combined With a Live Probiotic Tablet (Combined Bifidobacterium, Lactobacillus, Enterococcus and Bacillus Cereus Tablets, Live) in Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D)', 'source_field': 'protocolSection.identificationModule.officialTitle'}
Ingested At: 2026-10-31T23:27:35.664461+00:00
Published At: 2025-05-07T00:00:00+00:00
Record Updated At: 2025-05-07
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

protocolSection.conditionsModule.conditions: ["Irritable Bowel Syndrome", "Irritable Bowel Syndrome With Diarrhea (IBS-D)", "Repetitive Transcranial Magnetic Stimulation (rTMS)", "Probiotic", "Chronic Diarrhea", "Intestinal Flora"]
protocolSection.statusModule.lastUpdatePostDateStruct: {"date": "2025-05-07", "type": "ACTUAL"}
protocolSection.identificationModule.nctId: "NCT06960369"
protocolSection.identificationModule.officialTitle: "Efficacy of Repeated Transcranial Magnetic Stimulation Combined With a Live Probiotic Tablet (Combined Bifidobacterium, Lactobacillus, Enterococcus and Bacillus Cereus Tablets, Live) in Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D)"
protocolSection.statusModule.overallStatus: "RECRUITING"
protocolSection.designModule.phases: ["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct: null

{'armGroupLabels': ['rTMS combined with Live Probiotic tablet'], 'description': 'rTMS group received 1 Hz/s, 20 min for 2 week; Live Probiotic tablet group received tablets orally, 150 mg three times a day for 2 week.', 'name': 'rTMS combined with Live Probiotic tablet', 'type': 'COMBINATION_PRODUCT'} (protocolSection.armsInterventionsModule.interventions[])
{'armGroupLabels': ['rTMS combined placebo'], 'description': 'rTMS group received 1 Hz/s, 20 min for 2 week; placebo group received tablets orally, 150 mg three times a day for 2 week.', 'name': 'rTMS combined placebo', 'type': 'DEVICE'} (protocolSection.armsInterventionsModule.interventions[])
{'armGroupLabels': ['shamrTMS combined with Live Probiotic tablet'], 'description': 'Live Probiotic tablet group received tablets orally, 150 mg three times a day for 2 week, shamrTMS group received 0 Hz/s, 20 min for 2 week.', 'name': 'shamrTMS combined with Live Probiotic tablet', 'type': 'DRUG'} (protocolSection.armsInterventionsModule.interventions[])
{'armGroupLabels': ['shamrTMS combined placebo group'], 'description': 'shamrTMS group received 0 Hz/s, 20 min for 2 week; placebo group received tablets orally, 150 mg three times a day for 2 week.', 'name': 'shamrTMS combined placebo group', 'type': 'OTHER'} (protocolSection.armsInterventionsModule.interventions[])

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

A recorded drug name is not by itself an indication or a condition-specific relationship.

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