Success Metrics

Clinical Success Rate
50.0%

Based on 1 completed trials

Completion Rate
50%(1/2)
Active Trials
1(20%)
Results Posted
200%(2 trials)
Terminated
1(20%)

Phase Distribution

Ph not_applicable
4
80%

Phase Distribution

0

Early Stage

0

Mid Stage

0

Late Stage

Phase Distribution4 total trials
N/ANon-phased studies
4(100.0%)

Highest Phase Reached

Unknown

Trial Status & Enrollment

Completion Rate

33.3%

1 of 3 finished

Non-Completion Rate

66.7%

2 ended early

Currently Active

1

trials recruiting

Total Trials

5

all time

Status Distribution
Active(1)
Completed(1)
Terminated(2)
Other(1)

Detailed Status

Completed1
Recruiting1
Withdrawn1
unknown1
Terminated1

Development Timeline

Analytics

Development Status

Total Trials
5
Active
1
Success Rate
50.0%
Most Advanced
N/A

Trials by Phase

N/A4 (100.0%)

Trials by Status

completed120%
recruiting120%
withdrawn120%
unknown120%
terminated120%

Recent Activity

1 active trials
Showing 5 of 5
recruitingnot_applicable

FIBERGRAFT Aeridyan Posterolateral Fusion Study

NCT07059065
withdrawn

A Study Evaluating 3-Level OLIF Spine Fusion

NCT03896347
unknownnot_applicable

Demineralized Bone Matrix Rotator Cuff Study

NCT04686396
terminatednot_applicable

Human Amniotic Tissue-derived Allograft, NuCel, in Posteriolateral Lumbar Fusions for Degenerative Disc Disease

NCT02070484
completednot_applicable

Efficacy and Safety of Accell Evo3 Demineralized Bone Matrix (DBM) in Instrumented Posterolateral Lumbar Spine Fusion

NCT01430299

Clinical Trials (5)

Showing 5 of 5 trials
NCT07059065Not Applicable

FIBERGRAFT Aeridyan Posterolateral Fusion Study

Recruiting
NCT03896347

A Study Evaluating 3-Level OLIF Spine Fusion

Withdrawn
NCT04686396Not Applicable

Demineralized Bone Matrix Rotator Cuff Study

Unknown
NCT02070484Not Applicable

Human Amniotic Tissue-derived Allograft, NuCel, in Posteriolateral Lumbar Fusions for Degenerative Disc Disease

Terminated
NCT01430299Not Applicable

Efficacy and Safety of Accell Evo3 Demineralized Bone Matrix (DBM) in Instrumented Posterolateral Lumbar Spine Fusion

Completed

All 5 trials loaded

Drug Details

Intervention Type
DEVICE
Total Trials
5