# Safety, Efficacy, and Patient Preference of Split-Dose Crystalline Lactulose as a Preparation for Colonoscopy in Adults

> **NCT01650870** · PHASE2 · COMPLETED · sponsor: **Benaroya Research Institute** · enrollment: 40 (actual)

## Conditions studied

- Colonoscopy

## Interventions

- **DRUG:** Crystalline Lactulose

## Key facts

- **NCT ID:** NCT01650870
- **Lead sponsor:** Benaroya Research Institute
- **Sponsor class:** OTHER
- **Phase:** PHASE2
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2012-07
- **Primary completion:** 2012-09
- **Final completion:** 2012-09
- **Target enrollment:** 40 (ACTUAL)
- **Last updated:** 2014-08-08

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01650870

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01650870, "Safety, Efficacy, and Patient Preference of Split-Dose Crystalline Lactulose as a Preparation for Colonoscopy in Adults". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT01650870. Licensed CC0.

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