RecruitingPhase 4ACTRN12605000379617

Botulinum toxin injections into the salivary glands to reduce drooling in children

A randomised trial of botulinum toxin injections into the submandibular and parotid glands to reduce drooling in children with neurological disorders


Sponsor

Murdoch Children's Research Institute

Enrollment

56 participants

Start Date

Oct 1, 2004

Study Type

Interventional

Conditions

Summary

Children with cerebral palsy and other neurological impairments frequently have inadequate saliva control. The secretions may be odorous, cause chronic irritation of the facial skin and may damage clothing and books. Poor saliva control results in loss of self-esteem and can impede community inclusion. Conventional treatments include speech pathology intervention, the use of medication and surgical procedures. These interventions are not universally successful, and may be invasive (surgery) or lead to unwanted side effects (surgery and medication). There have been recent reports about the use of Botulinum toxin A (BTX-A), in the treatment of drooling. BTX-A is widely used as a treatment for spasticity in children with cerebral palsy, blocks the release of acetylcholine at the neuromuscular junction and selectively weakens the muscles for three to six months. This drug can be injected directly into the salivary glands under a general anaesthetic with ultrasound guidance. Within one to three days the drug binds on to the nerve endings and reduces the amount of saliva being produced from the injected salivary glands. Reports of the use of BTX-A are still limited with small groups of subjects, and include reports of studies in both adults and children, and also the injection of different combinations of glands in the various studies. The aim of our study is to assess the effectiveness of injections into the submandibular and parotid glands in a cohort of children with cerebral palsy and other neurological disorders. A randomised controlled study will be undertaken with children being allocated to either receive BTX-A at the start of the trial, or to a control group able to receive treatment at the conclusion of the six month study period. Measures will be undertaken at baseline for both groups, then at monthly intervals for six months. A sample size of 28 children per group will be required. Children will be recruited from the Saliva Control Clinic at the Royal Childrenÿ¿ÿ¢ÿ¿ÿ¿ÿ¿ÿ¿s Hospital and a cohort will also be recruited from the Monash Medical Centre (a separate ethics application will be made). BTX-A will then be injected into both submandibular and sublingual glands with ultrasound guidance. A short general anaesthetic will be necessary. Statistical analysis will be undertaken to determine the effectiveness of BTX-A in reducing poor saliva control. Adverse effects will be reported, and in particular, the views of parents will be established by means of a questionnaire.


Eligibility

Sex: Both males and femalesMin Age: 6 YearssMax Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This study is testing whether injecting botulinum toxin (Botox) into the salivary glands can reduce drooling in children with cerebral palsy and other neurological conditions. Many children with these conditions cannot control their saliva, which can cause skin irritation, social difficulties, and affect their quality of life. This injection temporarily reduces how much saliva the glands produce for several months. Researchers want to find out how effective and safe this treatment is. You may be eligible if: - Your child is between 6 and 18 years old - Your child has a significant problem with drooling - You (as the parent or guardian) understand the study requirements and are able to give consent You may NOT be eligible if: - Your child has previously received botulinum toxin injections to the salivary glands - Your child has had surgery to control drooling before - Your child has had any botulinum toxin treatment in the last 6 months - Your child is not healthy enough to have a general anaesthetic - You are unwilling to stop your child's drooling medication for the study period Talk to your doctor about whether this trial might be right for you.

This is a simplified summary. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

Single Injection of botulinum toxin A into submandibular and parotid glands (25 units per gland) x 1

Single Injection of botulinum toxin A into submandibular and parotid glands (25 units per gland) x 1


Locations(1)

Australia

View Full Details on ANZCTR

For the most up-to-date information, visit the official listing.

Visit

ACTRN12605000379617