Viewing Study NCT06172218



Ignite Creation Date: 2024-05-06 @ 7:53 PM
Last Modification Date: 2024-10-26 @ 3:16 PM
Study NCT ID: NCT06172218
Status: RECRUITING
Last Update Posted: 2023-12-15
First Post: 2023-12-07

Brief Title: AM for Refractory Achilles Tendinopathy
Sponsor: North Park Podiatry
Organization: North Park Podiatry

Study Overview

Official Title: Prospective Randomized Controlled Pilot Study Assessing Micronized Amniotic Membrane and Umbilical Cord Particulate in Patients With Symptomatic and Refractory Achilles Tendinopathy
Status: RECRUITING
Status Verified Date: 2023-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To evaluate outcomes after use of micronized amniotic membrane to replace or supplement damaged or inadequate integumental tissue in patients with chronic insertional or non-insertional Achilles tendinopathy that remains refractory to standard care Outcomes between a control and treatment group in this pilot study will be used to devise a multi-center study with larger sample size
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None