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Ultrasound-Guided Versus Anatomically Guided Botulinum Toxin Injection in Spasticity in Adults in Tanta University Hospitals

T

Tanta University

Status

Completed

Conditions

Spasticity
Botulinum Toxin
Adults
Ultrasound

Treatments

Drug: Botulinum toxin injection under anatomical landmark
Drug: Ultrasound-guided botulinum toxin injection

Study type

Observational

Funder types

Other

Identifiers

NCT06941883
36264MS248/7/23

Details and patient eligibility

About

This study aimed to compare the safety and outcome of ultrasound (US)- guided botulinum toxin (BoNT) injection and anatomically guided injection in muscle spasticity of different causes in adults.

Full description

One of the major complications of neurological diseases is spasticity which is defined as an increased velocity-dependent muscle tone.

A large volume of clinical data has demonstrated the efficacy and safety of botulinum toxin type A (BoNT-A) products for treating conditions such as spasticity.

Enrollment

68 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 18 years old.
  • Both sexes.
  • Patients with muscle spasticity.

Exclusion criteria

  • Patients with contraindications to botulinum toxin injection as allergy, myasthenia gravis, and cerebral palsy.

Trial design

68 participants in 2 patient groups

Botulinum toxin injection under anatomical landmark
Description:
Patients received botulinum toxin injections under the anatomical landmark.
Treatment:
Drug: Botulinum toxin injection under anatomical landmark
Ultrasound-guided botulinum toxin injection
Description:
Patients received ultrasound-guided botulinum toxin injection
Treatment:
Drug: Ultrasound-guided botulinum toxin injection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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