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NCT05546190 · ClinicalTrials.gov registry record

A Study to Collect Participants Experience of Living With Adult Upper Limb (AUL) Spasticity and to Assess the Arm Activity Measure (ArmA)

A clinical trial, sponsored by Ipsen.

Completed
Registry status
25
Enrollment target

NCT05546190: Completed study, sponsored by Ipsen.

NCT05546190 is a clinical trial that has completed, run by Ipsen. The registered enrollment target is 25 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05546190 has completed, sponsored by Ipsen.

COMPLETED
Registry status
25 participants
Enrollment target

Study Summary

The participants of this study will have AUL spasticity and have a need for botulinum toxin type A injections. AUL spasticity is where people develop tightening or stiffness of the muscles in the arms. Botulinum toxin type A is used for the treatment of spasticity in addition to physiotherapy. This study will ask participants to describe their experience living with AUL spasticity. This information will be used to assess the Arm Activity Measure (ArmA). ArmA is a scale designed to assess upper limb function in people with AUL spasticity. This study could suggest changes to the ArmA to improve its suitability for people with AUL spasticity or even the development of a new scale.

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2022-09-20
Est. Completion 2023-03-23
Ipsen

85 total trials

What the finished NCT05546190 record still lists

NCT05546190 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 25 participants, a relatively small participant target.

The record links to 0 conditions, and to 0 interventions.

NCT05546190 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05546190 about?

NCT05546190 is a clinical study titled "A Study to Collect Participants Experience of Living With Adult Upper Limb (AUL) Spasticity and to Assess the Arm Activity Measure (ArmA)". The participants of this study will have AUL spasticity and have a need for botulinum toxin type A injections. AUL spasticity is where people develop tightening or stiffness of the muscles in the arms. Botulinum toxin type A is used for the treatment of spasticity in addition to physiotherapy. This ...

What is the current status of trial NCT05546190?

This trial is currently completed. The enrollment target is 25 participants. The study started on 2022-09-20. Estimated completion is 2023-03-23.

Who is sponsoring clinical trial NCT05546190?

This trial is sponsored by Ipsen, which has 85 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT05546190, the US trial registry maintained by the National Library of Medicine. NCT05546190 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.