Clinical Trials Directory

Trials / Completed

CompletedNCT05625984

Study With Fascigel

Multi-centre, Open-label, First-in-man Study With Fascigel Used in Adult Patients Suffered From Back Pain

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
55 (actual)
Sponsor
Contipro Pharma a.s. · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The product is a Class III Medical Device. Structure is made by 1% sodium hyaluronate polysaccharide in normal saline solution. The device intended use is to help treat back pain by lubricating fascia.

Conditions

Interventions

TypeNameDescription
DEVICEFascigelThe product is a Class III Medical Device. Structure is made by 1% sodium hyaluronate polysaccharide in normal saline solution.

Timeline

Start date
2022-10-24
Primary completion
2023-11-13
Completion
2023-11-13
First posted
2022-11-23
Last updated
2024-02-07

Locations

3 sites across 1 country: Czechia

Source: ClinicalTrials.gov record NCT05625984. Inclusion in this directory is not an endorsement.

Study With Fascigel (NCT05625984) · Clinical Trials Directory