# In-vivo Efficacy Study of Patient Preoperative Preps

> **NCT01968356** · PHASE3 · TERMINATED · sponsor: **Solventum US LLC** · enrollment: 171 (actual)

## Conditions studied

- Skin Flora Bacterial Reduction Post-product Application

## Interventions

- **DRUG:** 3M CHG/IPA Prep Colorless
- **DRUG:** 3M CHG/IPA Prep Tint
- **DRUG:** ChloraPrep
- **DRUG:** Saline

## Key facts

- **NCT ID:** NCT01968356
- **Lead sponsor:** Solventum US LLC
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2013-10
- **Primary completion:** 2014-01
- **Final completion:** 2014-01
- **Target enrollment:** 171 (ACTUAL)
- **Why stopped:** Study discontinued due to data quality issues.
- **Last updated:** 2024-10-02

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01968356

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01968356, "In-vivo Efficacy Study of Patient Preoperative Preps". Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/clinical/NCT01968356. Licensed CC0.

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