# Lady Reading Hospital, Pakistan: Not applicable (device, behavioral) study in Severe Preeclampsia (434 participants)

**Score:** 30/100

| Field | Value |
|---|---|
| Sponsor | Lady Reading Hospital, Pakistan |
| Sponsor type | Non-US government |
| Study | Role of Postpartum Furosemide in Recovery of Patients With Severe Preeclampsia |
| NCT ID | NCT07861685 |
| Phase | Not applicable (device, behavioral) |
| Status | recruiting |
| Conditions | Severe Preeclampsia |
| Intervention types | drug |
| Target enrollment | 434 |
| Site countries | Pakistan |
| Posted | 2026-10-06 |
| Planned start | 2026-10-01 |
| Event | Newly registered study |
| Event date | 2026-10-06 |

## Why this score
- 434 participants planned.

Source: ClinicalTrials.gov (U.S. National Library of Medicine) API v2 (https://clinicaltrials.gov/study/NCT07861685). Last refreshed: 2026-11-04T06:04:38.232Z.
From public ClinicalTrials.gov registrations. Sponsor and study level only: we never list investigators, contacts or participants. A registration describes a planned study and can change. Status changes are read from each study's current status, actual dates and latest posted update, not a full change history, so an update can be a correction rather than a new change. Verify on ClinicalTrials.gov.