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NCT02052024 · ClinicalTrials.gov registry record · Phase 4

Myobloc Atrophy Study

A Phase 4 study, sponsored by Georgetown University.

Completed
Registry status
Phase 4
Development phase
10
Enrollment target

NCT02052024: Completed Phase 4 study, sponsored by Georgetown University.

NCT02052024 is a Phase 4 study that has completed, run by Georgetown University. The registered enrollment target is 10 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02052024, a Phase 4 study, has completed, sponsored by Georgetown University.

COMPLETED
Registry status
Phase 4
Development phase
10 participants
Enrollment target

Study Summary

The present pilot study is designed to assess the extent to which BOTOX and MYOBLOC cause muscle atrophy in spastic patients. The primary objective is to assess whether there is statistically significant difference in muscle atrophy between the two groups over a one year period.

Primary Outcome

The present pilot study is designed to assess the extent to which BTX-A (BOTOX) and BTX-B (MYOBLOC) cause muscle atrophy in spastic patients. The primary objective is to assess whether there is statistically significant difference in muscle atrophy between the two groups over a one-year period. Patient will complete a MRI of the tested muscle at baseline and at the end of the study. The MRI will be completed and read by the same radiologist throughout the study to account for inter rater variabi

Interventions

  • DRUG MYOBLOC
  • DRUG Botox

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2014-05
Est. Completion 2015-08
Phase Phase 4
Georgetown University

227 total trials

What the finished NCT02052024 record still lists

NCT02052024 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which MYOBLOC is the first listed.

NCT02052024 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02052024 about?

NCT02052024 is a clinical study titled "Myobloc Atrophy Study". The present pilot study is designed to assess the extent to which BOTOX and MYOBLOC cause muscle atrophy in spastic patients. The primary objective is to assess whether there is statistically significant difference in muscle atrophy between the two groups over a one year period.

What is the current status of trial NCT02052024?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 10 participants. The study started on 2014-05. Estimated completion is 2015-08.

What interventions are being tested in trial NCT02052024?

The interventions under investigation include: MYOBLOC (DRUG), Botox (DRUG).

Who is sponsoring clinical trial NCT02052024?

This trial is sponsored by Georgetown University, which has 227 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02052024's enrollment target sits among peer trials

10 1940th of 2000 higher than 33 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02052024, the US trial registry maintained by the National Library of Medicine. NCT02052024 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.