Evaluation of HQ® Matrix Soft Tissue Mesh for the Treatment of Inguinal Hernia
Multi-center, Randomized, Active-controlled, Single-blind, Parallel Two-group Trial of HQ® Matrix Soft Tissue Mesh and ULTRAPRO® Partially Absorbable Lightweight Mesh for the Treatment of Inguinal Hernia
Sponsor: Zhejiang Xingyue Biotechnology Co., Ltd.
A NA clinical study on Inguinal Hernia, this trial is ongoing. The trial is conducted by Zhejiang Xingyue Biotechnology Co., Ltd. and has accumulated 6 data snapshots since 2014. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
6 versions recorded-
Sep 2024 — Present [monthly]
Unknown NA
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Jul 2024 — Sep 2024 [monthly]
Unknown NA
Status: Unknown Status → Unknown
-
Jan 2021 — Jul 2024 [monthly]
Unknown Status NA
-
Jun 2018 — Jan 2021 [monthly]
Unknown Status NA
-
Jul 2017 — Jun 2018 [monthly]
Unknown Status NA
Status: Recruiting → Unknown Status
▶ Show 1 earlier version
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Jan 2017 — Jul 2017 [monthly]
Recruiting NA
First recorded
Nov 2014
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Zhejiang Xingyue Biotechnology Co., Ltd.
For direct contact, visit the study record on ClinicalTrials.gov .