# U-CaVIT Versus Standard of Care for Prevention of Atonic Postpartum Hemorrhage After Cesarean Section in High-risk Women.

> **NCT07019623** · NA · RECRUITING · sponsor: **Christian Haslinger** · enrollment: 70 (estimated)

## Conditions studied

- Postpartum Hemorrhage (Primary)
- Hemorrhage
- Postpartum Complication
- Delivery ,Complications,Maternal
- Pregnancy Complications
- Cesarean Delivery
- Balloon

## Interventions

- **DEVICE:** Rüsch® Balloon Catheter Ch. 24
- **OTHER:** Ultrasonography

## Key facts

- **NCT ID:** NCT07019623
- **Lead sponsor:** Christian Haslinger
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2025-05-28
- **Primary completion:** 2026-11
- **Final completion:** 2026-11
- **Target enrollment:** 70 (ESTIMATED)
- **Last updated:** 2026-04-22

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07019623

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07019623, "U-CaVIT Versus Standard of Care for Prevention of Atonic Postpartum Hemorrhage After Cesarean Section in High-risk Women.". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT07019623. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
