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Comparative Trial of Botox in the Management of Children With Congenital Muscular Torticollis

University of British Columbia logo

University of British Columbia

Status and phase

Withdrawn
Phase 1

Conditions

Torticollis

Treatments

Drug: Botox

Study type

Interventional

Funder types

Other

Identifiers

NCT00175604
C03-0550
W03-0164

Details and patient eligibility

About

The primary purpose is to investigate the effect of Botox on the treatment of congenital muscular torticollis (CMT). The investigators' hypothesis is that a Botox injection will be an effective treatment when used in conjunction with current treatment procedures.

Full description

The babies that require a neck collar for CMT will be randomly placed into two groups. One group will receive standard treatment which includes physiotherapy and occupational therapy. The other group will receive standard treatment plus an injection of Botox. The babies will be monitored to determine if one group has a more favorable outcome than the other in terms of range of motion, length of treatment time and number of required surgeries.

Sex

All

Ages

4 months to 1 year old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Infants diagnosed with CMT and referred by family physician, pediatrician or orthopaedic surgeon
  • Initial assessment and initiation of treatment prior to 4 months of age
  • Cervical spine radiograph, no focal bony abnormality
  • Head tilt greater than 5 degrees at 5 months of age
  • Lateral head righting past neutral in upright suspension
  • Restricted neck range of movement in lateral flexion or rotation or both
  • Signed consent form and willingness to participate in the study
  • Compliance with attending bi-weekly follow-up appointments

Exclusion criteria

  • Any other diagnosis affecting tone or muscle function
  • Any condition that would preclude an anesthetic
  • Any vertebral abnormalities identified by radiograph
  • Attending other health practitioners for treatment, i.e., massage therapist, chiropractor
  • Any associated ocular problems as determined by a pediatric ophthalmologist

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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