# In-vivo Efficacy Study of Patient Pre-operative Preps

> **NCT01968707** · PHASE3 · COMPLETED · sponsor: **Solventum US LLC** · enrollment: 426 (actual)

## Conditions studied

- Bacterial Reduction on Skin Flora Post-product Application

## Interventions

- **DRUG:** ChloraPrep Hi-Lite Orange
- **DRUG:** Normal saline
- **DRUG:** 3M CHG/IPA Prep Tint 10.5-mL
- **DRUG:** 3M CHG/IPA Prep Tint 26-mL

## Key facts

- **NCT ID:** NCT01968707
- **Lead sponsor:** Solventum US LLC
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2013-10
- **Primary completion:** 2014-06
- **Final completion:** 2014-06
- **Target enrollment:** 426 (ACTUAL)
- **Last updated:** 2024-10-02

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01968707

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01968707, "In-vivo Efficacy Study of Patient Pre-operative Preps". Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/clinical/NCT01968707. Licensed CC0.

---

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