# Safety and Efficacy Study of Regen Sling to Treatment SUI

> **NCT02106299** · PHASE3 · UNKNOWN · sponsor: **Medprin Regenerative Medical Technologies Co., Ltd.** · enrollment: 178 (estimated)

## Conditions studied

- Stress Urinary Incontinence

## Interventions

- **DEVICE:** Regen sling
- **DEVICE:** tension-free vaginal tape-obturator(TVT-O)

## Key facts

- **NCT ID:** NCT02106299
- **Lead sponsor:** Medprin Regenerative Medical Technologies Co., Ltd.
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2014-01
- **Primary completion:** 2014-12
- **Final completion:** 2015-12
- **Target enrollment:** 178 (ESTIMATED)
- **Last updated:** 2014-04-08


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02106299

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02106299, "Safety and Efficacy Study of Regen Sling to Treatment SUI". Retrieved via AI Analytics 2026-06-23 from https://api.ai-analytics.org/clinical/NCT02106299. Licensed CC0.

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