Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05796765 · ClinicalTrials.gov registry record · Phase 2

Phase 2B Micronized DHACM vs. Saline in the Treatment of Knee Osteoarthritis

A Phase 2 study, sponsored by MiMedx Group.

Terminated
Registry status
Phase 2
Development phase
43
Enrollment target

NCT05796765 is a Phase 2 study that was terminated before completion, run by MiMedx Group. The registered enrollment target is 43 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05796765, a Phase 2 study, was terminated before completion, sponsored by MiMedx Group.

TERMINATED
Registry status
Phase 2
Development phase
43 participants
Enrollment target

Study Summary

The purpose of this study is to determine the safety and efficacy of the 40 mg and 100 mg doses of allogeneic micronized dehydrated human amnion/chorion membrane (micronized DHACM) injectable compared to 0.9% sodium chloride injection, placebo control for the treatment of knee osteoarthritis

Interventions

  • DRUG Saline
  • BIOLOGICAL Micronized DHACM 40 mg
  • BIOLOGICAL Micronized DHACM 100 mg

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2023-03-24
Est. Completion 2023-12-15
Phase Phase 2

Sponsor

MiMedx Group

32 total trials

What the Registry Record Tells You About NCT05796765

The ClinicalTrials.gov registry entry for NCT05796765 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 43 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is MiMedx Group, which has 32 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Saline is the first listed.

NCT05796765 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05796765 about?

NCT05796765 is a clinical study titled "Phase 2B Micronized DHACM vs. Saline in the Treatment of Knee Osteoarthritis". The purpose of this study is to determine the safety and efficacy of the 40 mg and 100 mg doses of allogeneic micronized dehydrated human amnion/chorion membrane (micronized DHACM) injectable compared to 0.9% sodium chloride injection, placebo control for the treatment of knee osteoarthritis

What is the current status of trial NCT05796765?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 43 participants. The study started on 2023-03-24. Estimated completion is 2023-12-15.

What interventions are being tested in trial NCT05796765?

The interventions under investigation include: Saline (DRUG), Micronized DHACM 40 mg (BIOLOGICAL), Micronized DHACM 100 mg (BIOLOGICAL).

Who is sponsoring clinical trial NCT05796765?

This trial is sponsored by MiMedx Group, which has 32 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.