# Study Evaluating the Impact of Mesh Pore Size on Chronic Pain After Lichtenstein Hernioplasty

> **NCT02500056** · NA · COMPLETED · sponsor: **Tartu University Hospital** · enrollment: 143 (actual)

## Conditions studied

- Inguinal Hernia

## Interventions

- **DEVICE:** Optilene LP mesh
- **DEVICE:** Ultrapro mesh

## Key facts

- **NCT ID:** NCT02500056
- **Lead sponsor:** Tartu University Hospital
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2011-01
- **Primary completion:** 2012-04
- **Final completion:** 2015-04
- **Target enrollment:** 143 (ACTUAL)
- **Last updated:** 2017-07-11


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02500056

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02500056, "Study Evaluating the Impact of Mesh Pore Size on Chronic Pain After Lichtenstein Hernioplasty". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT02500056. Licensed CC0.

---

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