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New combo therapy eases stroke arm stiffness

NCT ID NCT07624149

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at 39 adults who had arm stiffness (spasticity) after a stroke. Researchers compared different types of transcranial magnetic stimulation (TMS) combined with Botox injections to see which worked best. The goal was to reduce muscle tightness and improve arm movement and daily activities.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

39 people

The number who actually took part.

Started

Jan 2025

Finished

May 2026

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 80 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Diagnosis of stroke (ischemic or hemorrhagic) * Time since stroke onset between 3 and 24 months * Age between 18 and 80 years * Upper extremity motor recovery at Brunnstrom Stages 3-5 * Spasticity in the elbow, wrist, or finger flexor muscle groups of the upper extremity with a Modified Ashworth Scale (MAS) score between +1 and 3 * Receipt of botulinum toxin-A injection to the affected upper extremity within the previous week Exclusion Criteria: * History of epileptic seizures, epileptiform EEG findings, increased seizure risk, or use of antiepileptic medication * Presence of implanted metallic or electronic devices (e.g., cardiac pacemaker, intrathecal baclofen pump) * Pregnancy or lactation * Presence of neurological disorders other than stroke * History of cranial surgery * Orthopedic conditions or previous orthopedic surgery limiting upper extremity movement * Severe upper extremity spasticity (MAS \>3) or presence of contracture * Uncontrolled hypertension, advanced heart failure (NYHA Class III-IV), chronic obstructive pulmonary disease (COPD), active infection, severe hepatic failure, or severe renal failure * History of malignancy * Severe cognitive impairment (Mini-Mental State Examination score \<24) * Severe aphasia or communication disorder that would interfere with participation in the study * Botulinum toxin injection administered to the upper extremity in a separate treatment session within the previous 3 months * Any change in medication type or dosage within the previous month for oral medications used in the management of spasticity

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Ankara Etlik City Hospital, Physical Medicine and Rehabilitation Clinic

    Ankara, Ankara, 06010, Turkey (Türkiye)