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NCT01621113 · ClinicalTrials.gov registry record · Phase 2

Combination Therapy With Dalfampridine and Locomotor Training for Chronic, Motor Incomplete Spinal Cord Injury

A Phase 2 study, sponsored by Kessler Foundation.

Completed
Registry status
Phase 2
Development phase
27
Enrollment target

NCT01621113: Completed Phase 2 study, sponsored by Kessler Foundation.

NCT01621113 is a Phase 2 study that has completed, run by Kessler Foundation. The registered enrollment target is 27 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01621113, a Phase 2 study, has completed, sponsored by Kessler Foundation.

COMPLETED
Registry status
Phase 2
Development phase
27 participants
Enrollment target

Study Summary

The purpose of this study is to determine the efficacy, safety, and tolerability of treatment with dalfampridine in combination with locomotor training in persons with chronic, motor incomplete SCI.

Primary Outcome

The 6MWT measures the distance (in meters) walked within 6 minutes. The test is a measure of endurance; however, can also be used to measure walking speed.

Interventions

  • DRUG Placebo
  • DRUG Dalfampridine

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2012-06
Est. Completion 2017-10-16
Phase Phase 2
Kessler Foundation

104 total trials

What the finished NCT01621113 record still lists

NCT01621113 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (80% lower).

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

NCT01621113 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01621113 about?

NCT01621113 is a clinical study titled "Combination Therapy With Dalfampridine and Locomotor Training for Chronic, Motor Incomplete Spinal Cord Injury". The purpose of this study is to determine the efficacy, safety, and tolerability of treatment with dalfampridine in combination with locomotor training in persons with chronic, motor incomplete SCI.

What is the current status of trial NCT01621113?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 27 participants. The study started on 2012-06. Estimated completion is 2017-10-16.

What interventions are being tested in trial NCT01621113?

The interventions under investigation include: Placebo (DRUG), Dalfampridine (DRUG).

Who is sponsoring clinical trial NCT01621113?

This trial is sponsored by Kessler Foundation, which has 104 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01621113's enrollment target sits among peer trials

27 1697th of 2000 higher than 293 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT01621113, the US trial registry maintained by the National Library of Medicine. NCT01621113 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.