# Study to Evaluate the Effectiveness of the Initial Specimen Diversion Device

> **NCT02102087** · NA · COMPLETED · sponsor: **Magnolia Medical Technologies, Inc.** · enrollment: 971 (actual)

## Conditions studied

- Septicemia

## Interventions

- **DEVICE:** Initial Specimen Diversion Device (ISDD)
- **DEVICE:** Lab standard practice (LSP)

## Key facts

- **NCT ID:** NCT02102087
- **Lead sponsor:** Magnolia Medical Technologies, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2014-07
- **Primary completion:** 2015-10
- **Final completion:** 2015-10
- **Target enrollment:** 971 (ACTUAL)
- **Last updated:** 2017-08-11


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02102087

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02102087, "Study to Evaluate the Effectiveness of the Initial Specimen Diversion Device". Retrieved via AI Analytics 2026-06-16 from https://api.ai-analytics.org/clinical/NCT02102087. Licensed CC0.

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