Registry-listed formulations

This catalogue entry has no confirmed scientific concept.

Each study is counted once in the molecule profile. Registry products remain separate. Naming an ingredient does not establish that products are interchangeable or what participants received.

0 source entries across 0 studies. This list may not include all unresolved or historical entries.

    Success Metrics

    Clinical Success Rate
    100.0%

    Based on 1 completed trials

    Completion Rate
    100%(1/1)
    Active Trials
    0(0%)
    Results Posted
    0%(0 trials)

    Phase Distribution

    Not Applicable
    2
    67%

    Phase Distribution

    0

    Early Stage

    0

    Mid Stage

    0

    Late Stage

    Phase Distribution2 total trials
    N/ANon-phased studies
    2(100.0%)

    Highest Phase Reached

    Unknown

    Trial Status & Enrollment

    Completion Rate

    50.0%

    1 of 2 finished

    Non-Completion Rate

    50.0%

    1 ended early

    Currently Active

    0

    trials recruiting

    Total Trials

    3

    all time

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

    Detailed Status

    Completed1
    unknown1
    Withdrawn1

    Development Timeline

    Analytics

    Development Status

    Total Trials
    3
    Active
    0
    Success Rate
    100.0%
    Most Advanced
    N/A

    Trials by Phase

    N/A2 (100.0%)

    Trials by Status

    completed133%
    unknown133%
    withdrawn133%

    Recent Activity

    0 active trials
    Showing 3 of 3
    unknownnot_applicable

    Minimal Invasive Deformity Correction (MID-C) System for Early Onset Scoliosis

    NCT03519321
    withdrawnnot_applicable

    Limited-efficacy Testing of Spring Distraction System (SDS) and Unilateral One-way Rod (MID-C) for Early Onset Scoliosis

    NCT04003233
    completed

    Feasibility Evaluation Study of the MID-C Device

    NCT03071471

    Clinical Trials (3)

    Showing 3 of 3 trials
    NCT03519321Not Applicable

    Minimal Invasive Deformity Correction (MID-C) System for Early Onset Scoliosis

    Unknown
    NCT04003233Not Applicable

    Limited-efficacy Testing of Spring Distraction System (SDS) and Unilateral One-way Rod (MID-C) for Early Onset Scoliosis

    Withdrawn
    NCT03071471

    Feasibility Evaluation Study of the MID-C Device

    Completed

    All 3 trials loaded

    Drug Details

    Intervention Type
    Device
    Total Trials
    3