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NCT07288801RecruitingPhase 4

Vitamin D for Preventing Recurrent Preeclampsia in Pregnant Women

Role of Vitamin D in Prevention of Preeclampsia Recurrence in Pregnant Women With Previous History of Preeclampsia: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 17 Dec 2025

Brief summary (registry, in English)

The goal of this clinical trial is to find out whether giving vitamin D to pregnant women who had pre-eclampsia in a previous pregnancy helps prevent the condition from coming back. The main question it aims to answer is: Does vitamin D supplementation reduce the chance of pre-eclampsia recurring in pregnant women with a history of pre-eclampsia? To answer this question, pregnant women attending the antenatal clinic at the Department of Obstetrics and Gynaecology, Nishtar Hospital Multan will be invited to join the study. Participants will be randomly assigned to two equal groups: * Vitamin D group: will take 4,000 IU of oral vitamin D until 36 weeks of gestation. * Placebo group: will receive a pill identical in appearance, taste, and consistency but without vitamin D. While on the study medication, each woman will visit the clinic every two weeks. At each visit, her blood pressure will be measured, and if it is 140/90 mmHg or higher, a urine test will check for protein to identify pre-eclampsia as per hospital protocol. Any diagnosis of pre-eclampsia will lead to standard care, and the outcome will be recorded. At the end, researchers will compare how many women in each group developed recurrent pre-eclampsia. This study will help answer whether vitamin D supplementation can safely reduce the risk of pre-eclampsia returning in women with a prior history - a question important for improving pregnancy outcomes and maternal health.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
146 (estimated)
First submitted
4 Dec 2025
Start date
9 Aug 2025
Primary completion date
8 Feb 2026
Lead sponsor
Nishtar Medical University
NCT number
NCT07288801

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 146
  • From 9 Aug 2025 to the primary completion date, 8 Feb 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Pre-existing hypertension, cardiac diseases, renal disease, thyrotoxicosis (on history and medical record)

Other

  • Women presenting with intra-uterine death of the fetus.

Who the study is looking for

  • Gestational age ≥ 20-weeks (on LMP method) ' - Past medical history of pre-eclampsia

Age in the registry: 20 years to 45 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Nishtar Medical University and Hospital
Coordinator of this site? Confirm its status
MultanPakistanRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.