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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05615987
Other study ID # 2022-01-14
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received
Last updated
Start date December 1, 2022
Est. completion date October 1, 2023

Study information

Verified date November 2022
Source Konya Beyhekim Training and Research Hospital
Contact Savas Karpuz, M.D.
Phone +905552057860
Email svskrpz@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to compare the effectiveness of the classical (2-4 points to the muscle proximal) application of botulinum toxin in the treatment of spasticity with the application along the length of the gastrecnemius muscle. The main question it aims to answer Is botulinum toxin more effective in the treatment of spasticity than the classical application applied along the length of the gastrocnemius muscle? Participants will be evaluated for spasticity before and 1 month after injection. Researchers will compare classical versus application along the length of the muscle to see if there is a reduction in spasticity.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date October 1, 2023
Est. primary completion date September 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Diagnosed with spastic hemiplegia - Spasticity in the gastrocnemius muscle Exclusion Criteria: - Those who have spasticity in other muscles that will affect ankle movements - Those who use myorelaxant or myospasm-effective drugs - Those who have been applied botulinum toxin in the last 3 months - Those who have contractures in the ankle and knee due to orthopedic reasons.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Onabotulinumtoxina for Injection
200iu/2ml in both groups

Locations

Country Name City State
Turkey Konya Beyhekim Research and Training Hospital Konya Selçuklu

Sponsors (1)

Lead Sponsor Collaborator
Konya Beyhekim Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (6)

Childers MK, Kornegay JN, Aoki R, Otaviani L, Bogan DJ, Petroski G. Evaluating motor end-plate-targeted injections of botulinum toxin type A in a canine model. Muscle Nerve. 1998 May;21(5):653-5. — View Citation

Kaymak B, Kara M, Tok F, Ulasli AM, Öztürk GT, Chang KV, Hsiao MY, Hung CY, Yagiz On A, Özçakar L. Sonographic guide for botulinum toxin injections of the lower limb: EUROMUSCULUS/USPRM spasticity approach. Eur J Phys Rehabil Med. 2018 Jun;54(3):486-498. doi: 10.23736/S1973-9087.17.04667-6. Epub 2017 Apr 4. Review. — View Citation

Kim MW, Kim JH, Yang YJ, Ko YJ. Anatomic localization of motor points in gastrocnemius and soleus muscles. Am J Phys Med Rehabil. 2005 Sep;84(9):680-3. — View Citation

Prodanov D, Nagelkerke N, Marani E. Spatial clustering analysis in neuroanatomy: applications of different approaches to motor nerve fiber distribution. J Neurosci Methods. 2007 Feb 15;160(1):93-108. Epub 2006 Oct 17. — View Citation

Prodanov D, Thil MA, Marani E, Delbeke J, Holsheimer J. Three-dimensional topography of the motor endplates of the rat gastrocnemius muscle. Muscle Nerve. 2005 Sep;32(3):292-302. — View Citation

Shaari CM, Sanders I. Quantifying how location and dose of botulinum toxin injections affect muscle paralysis. Muscle Nerve. 1993 Sep;16(9):964-9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Spasticity assessment (change between pre-injection and 1-month control) Modified ashworth scale before injection and 1 month after injection
Primary Spasticity assessment (change between pre-injection and 1-month control) Tardieu scale before injection and 1 month after injection
Primary Spasticity assessment (change between pre-injection and 1-month control) Joint range of motion measurement before injection and 1 month after injection
Primary ambulation level (change between pre-injection and 1-month control) functional ambulation scale before injection and 1 month after injection
Primary ambulation velocity (change between pre-injection and 1-month control) preferred walking speed before injection and 1 month after injection
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