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Active, not recruitingNCT06548321Updated Aug 12, 2024

Benefits of Extracorporeal Shockwave Therapy to Reduce Spasticity in Stroke/CP

An interventional study of Extracorporeal Shockwave Therapy in Stroke, Cerebral, sponsored by Superior University. Active, not recruiting at 1 site in Pakistan. Open to participants aged 10 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-08-12.

Sponsored by Superior University · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Registered 10 months after the study started (first participant enrolled Oct 2023, registered Aug 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
28
Allocation
Not applicable
Ages
10 Years to 50 Years
Sex
All
01

Study summary

This Study will help to explain us that ExtracorporealShockwave therapy can reduce spasticity in Stroke Patient,help them to restore their abilities and ROM.Therapy reduces dependency rate of patient.Also seen this therapy shows reduction in spasticity of CP child population.Improving the motor recovery.

Read the detailed description

ESWT therapy increses molecular and immunological reactions,increase blood microcirculation and neurovascularization.It enhancing the neural proliferation of neural stem cell(NSC),which shows repair in brain function in CNS diseases.Extracorporeal shockwave can produce Nitric oxide in enzymatic and non enzymatic way which help, to reduce muscle spasm.Extracorporeal Shockwave reduce the exitibilty of motor neuron by vibratory stimulation of tendon and reduces tension.After 2 weeks ESWT muscle tension reduces increases range of motion reduces the pain.shock wave therapy appears to be effective in reducing spasticity levels irrespective of the age of the participants, the type of injury, and the tool used to measure the effect.ESWT change in motor neuron exitibilty \& also associated with the spastic muscle.

02

Conditions studied

  • Stroke, Cerebral

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03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,013 are open to participants now.

This study's enrollment of 28 is below the median of 50 across 5,366 interventional studies indexed under Stroke.

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Lead sponsor

Superior University is the lead sponsor of 242 studies on the registry; 24 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
10 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 3rd stage of Stroke

Exclusion criteria

Exclusion Criteria:

  • Non spastic CP,1st stage of Stroke,Spasticity caused by injury,Newborn
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Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
28 participants (actual)

Study arms

  • Experimental
    Extracorporeal Shockwave Therapy

    Diagnostic Test: Extracorporeal Shockwave Therapy

Interventions

  • Diagnostic testExtracorporeal Shockwave Therapy

    " The ESTW machine is turned on and the instrument, or shockwave gun, is pressed against the affected area. Rapid impulses are then delivered to the patient. Treatment typically lasts between 5 and 15 minutes. While this treatment can be uncomfortable for some, most do not experience any pain. Once treatment is completed, patients should do their best to physical activity... higher levels of energy Shockwaves into deeper tissue locations... ESWT therapies can help treat neurological disorders like multiple sclerosis and the effects of stroke.

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What researchers measure

Primary outcomes

  1. Modified Ashworth Scale MAS

    The Ashworth Scale method of grading spasticity, working with Cerebral Palsy and Stroke patients. The original Ashworth scale was a 5 point numerical scale that graded spasticity from 0 to 4, with 0 being no resistance and 4 being a limb rigid in flexion or extension. In 1987, while performing a study to exam interrater reliability of manual tests of elbow flexor muscle spasticity, Bohannon and Smith modified the Ashworth scale by adding 1+ to the scale to increase sensitivity. Since its modification, the modified Ashworth scale (MAS), has been applied in clinical practice and research as a measure of spasticity.

    Time frame: 12 Months

07

Study locations

1 site
  • Clinical setups Sargodha,Lahore,BWN
    Lahore, Pakistan
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 12, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06548321
Lead sponsor
Superior University
Responsible party
Muhammad Naveed Babur (Principal Investigator, Superior University) — Principal investigator
First posted
Aug 12, 2024
Start date
Oct 1, 2023
Primary completion
May 1, 2024
Completion
Sep 30, 2024 (estimated)
Last update
Aug 12, 2024

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Aug 2024. You cannot join it, but the record below documents what was studied.

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