# A Clinical Study for Validating the Equivalence of Bloomlife MFM-Pro to Clinical Standard-of-care for Antepartum Fetal Monitoring

> **NCT05060172** · NA · COMPLETED · sponsor: **Bloom Technologies** · enrollment: 96 (actual)

## Conditions studied

- Fetal Monitoring

## Interventions

- **DEVICE:** Bloomlife MFM-Pro

## Key facts

- **NCT ID:** NCT05060172
- **Lead sponsor:** Bloom Technologies
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2021-06-25
- **Primary completion:** 2021-11-09
- **Final completion:** 2021-11-25
- **Target enrollment:** 96 (ACTUAL)
- **Last updated:** 2022-01-25


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05060172

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05060172, "A Clinical Study for Validating the Equivalence of Bloomlife MFM-Pro to Clinical Standard-of-care for Antepartum Fetal Monitoring". Retrieved via AI Analytics 2026-06-01 from https://api.ai-analytics.org/clinical/NCT05060172. Licensed CC0.

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