CLINICAL_TRIALS
ClinicalTrials.gov record update
Under Pressure: Arugula Extract's Effect on Blood Pressure in Hypertensive Individuals
This page presents selected fields from the linked source record. It does not add a medical interpretation.
Record identity and dates
- Source
- ClinicalTrials.gov
- Source record ID
- NCT07904832
- Title field or adapter rule
- {'original_value': "Under Pressure: Arugula Extract's Effect on Blood Pressure in Hypertensive Individuals", 'source_field': 'protocolSection.identificationModule.officialTitle'}
- Ingested At
- 2026-10-31T23:27:31.779742+00:00
- Published At
- 2026-10-29T00:00:00+00:00
- Record Updated At
- 2026-10-29
- Source Retrieved At
- 2026-10-31T22:18:32.315169+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
["Hypertension (HTN)", "Hypertension"]- protocolSection.statusModule.lastUpdatePostDateStruct
{"date": "2026-10-29", "type": "ACTUAL"}- protocolSection.identificationModule.nctId
"NCT07904832"- protocolSection.identificationModule.officialTitle
"Under Pressure: Arugula Extract\u0027s Effect on Blood Pressure in Hypertensive Individuals"- protocolSection.statusModule.overallStatus
"COMPLETED"- protocolSection.designModule.phases
["NA"]- protocolSection.statusModule.resultsFirstPostDateStruct
null
Study condition terms
Interventions recorded in this study
- {'armGroupLabels': ['Arugula Extract Followed by Placebo'], 'description': 'Participants consume a single oral dose of 4,000 mg arugula extract (AE), providing approximately 400 mg of dietary nitrate (10% nitrate concentration). Arugula Extract is administered in capsule form following baseline cardiovascular and vascular assessments. Blood pressure, heart rate, and blood biomarkers are assessed at baseline, 1, 2, 3, and 24 hours following supplementation. Flow-mediated dilation is assessed at baseline, 3 hours, and 24 hours.', 'name': 'Arugula Extract', 'type': 'DIETARY_SUPPLEMENT'} (protocolSection.armsInterventionsModule.interventions[])
- {'armGroupLabels': ['Placebo Followed by Arugula Extract'], 'description': 'Participants consume a single oral dose of 4,000 mg psyllium husk as the placebo condition. The placebo is administered in capsule form following baseline cardiovascular and vascular assessments. Blood pressure, heart rate, and blood biomarkers are assessed at baseline, 1, 2, 3, and 24 hours following supplementation. Flow-mediated dilation is assessed at baseline, 3 hours, and 24 hours.', 'name': 'Psyllium Husk', 'type': 'DIETARY_SUPPLEMENT'} (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.