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Pre Eclampsia, Severe / Hypertensive Disorder of Pregnancy / Low Sodium Diet · Interventional Study
ClinicalTrials.gov · August 7, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a planned randomized controlled trial registered prospectively to evaluate whether a low-sodium diet (<2000 mg/day) reduces mean arterial blood pressure on postpartum day 7 in women with late-onset hypertensive disorder of pregnancy. No results are available; recruitment has not yet begun.
Interventional, Randomized, Parallel, Open label, Treatment purpose. Hypertensive Disorder of Pregnancy, Pre-Eclampsia, Severe, Pre-Eclampsia; Mild, Postpartum; Female; age from 18 Years. Intervention: Low-Sodium Diet. Compared with: Regular Diet — No Intervention. n = 110. Women and Infants Hospital of Rhode Island (lead sponsor); no multicentre sites disclosed..
This is a planned randomized controlled trial registered prospectively to evaluate whether a low-sodium diet (<2000 mg/day) reduces mean arterial blood pressure on postpartum day 7 in women with late-onset hypertensive disorder of pregnancy. No results are available; recruitment has not yet begun.
No results, safety data, efficacy data, or recruitment details are reported in this registry record.
If completed and positive, this trial would address a gap in evidence regarding dietary sodium reduction as a non-pharmacological intervention for postpartum blood pressure management. Results are not yet available and the trial is not yet recruiting.
This is a clinical trial registry record with no results posted; the study is not yet recruiting and therefore provides no evidence of efficacy or safety.
As stated by the source record.
Quoted from the source exactly as published.
If completed and positive, this trial would address a gap in evidence regarding dietary sodium reduction as a non-pharmacological intervention for postpartum blood pressure management. Results are not yet available and the trial is not yet recruiting.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT07752056). This is a study registration, not published results. Lead sponsor: Women and Infants Hospital of Rhode Island. Recruitment status: NOT_YET_RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 110 participants (ESTIMATED). Conditions: Hypertensive Disorder of Pregnancy, Pre-Eclampsia, Severe, Pre-Eclampsia; Mild, Postpartum. Interventions: OTHER: Low Sodium Diet. Primary outcome measures: Difference in Mean Arterial Blood Pressure (MAP) on Postpartum Day 7 , 7 days following delivery. Brief summary: The goal of this randomized controlled trial is to learn if a low-sodium diet improves postpartum blood pressure control in adults who were diagnosed with a late-onset hypertensive disorder of pregnancy. The main questions it aims to answer are: * Does a low-sodium diet lead to decreased mean arterial blood pressure (MAP) on postpartum day 7? * Does a low-sodium diet lead to a decreased MAP on postpartum day 3? * Does a low-sodium diet reduce 30-day hospital readmissions for hypertension-related indications? Participants will be provided with meals for 7 days following their delivery. The experimental diet will contain less than 2000mg of sodium daily. The control diet will have variable sodium content with no restrictions. Participants will be asked to record the food they consume over the study week. They will also be provided with a blood pressure (BP) cuff and asked to record their BP at least once daily.
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.