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Completed Phase 3 Interventional Results available

Efficacy and Safety Study of Botulinum Toxin Type A Against Placebo to Treat Spasticity in the Arm After a Stroke

ClinicalTrials.gov ID: NCT01392300

Public ClinicalTrials.gov record NCT01392300. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 9:56 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Prospective, Double-blind, Placebo-controlled, Randomized, Multi-center Study With an Open-label Extension Period to Investigate the Efficacy and Safety of NT 201 in the Treatment of Post-stroke Spasticity of the Upper Limb

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine whether injections of Botulinum toxin type A into muscles of the upper limb are effective in treating spasticity in patients after stroke.

Study identification

NCT ID
NCT01392300
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Merz Pharmaceuticals GmbH
Industry
Enrollment
317 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2011 (Type not available)
Primary completion
Mar 2013 (Actual)
Completion
Feb 2014 (Actual)
Last update posted
Jan 16, 2017

2011 – 2014

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Merz Investigational Site #001184 Downey California 90242 —
Merz Investigational Site #001017 Fountain Valley California 92728 —
Merz Investigational Site #001188 Miami Florida 33172 —
Merz Investigational Site #001037 Augusta Georgia 30912 —
Merz Investigational Site #001186 Chicago Illinois 60611 —
Merz Investigational Site # 001110 Overland Park Kansas 66211 —
Merz Investigational Site #001198 Stratford New Jersey 08084 —
Merz Investigational Site #001240 Chapel Hill North Carolina 27599 —
Merz Investigational Site #001009 Winston-Salem North Carolina 27157 —
Merz Investigational Site #001241 Philadelphia Pennsylvania 19140 —
Merz Investigational Site #001211 Pittsburgh Pennsylvania 15213 —
Merz Investigational Site #001245 Chattanooga Tennessee 37403 —
Merz Investigational Site #001226 Houston Texas 77030 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 34 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01392300, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 16, 2017 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01392300 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →