Clinical Trials Logo

Clinical Trial Summary

A 100 units of botulinum toxin was injected in both parotid and submandibular glands for children (2 - 12 years) with incapacitating sialorrhea in juvenile cerebral palsy patients and they are followed up for 1 year


Clinical Trial Description

This was a prospective, longitudinal analysis with 1-year follow-up of 52 children with juvenile cerebral palsy (JCP) suffering from sialorrhea enrolled from 3 tertiary pediatric neurology rehabilitation centers (two in Cairo and one in Alexandria) and subjected to repeated BoNT-A injection. The recruitment period was between June 30, 2021, until May 1, 2022 (the last patient follow-up ended on April 30, 2023). Intervention: 100 units of OnabotulinumtoxinA (Botox®) were injected in the parotid and submandibular glands Follow-up visits: mo 1 post-injection (for every injection session) and every 3 months thereafter In each visit; the following efficacy variables were assessed: Primary outcome measures: The severity and frequency of sialorrhea evaluated by Drooling Severity Scale (DSS), and Drooling Frequency Scale (DFS) and visual-analogic ratings of familial distress (VAS-FD). Secondary outcome measure: The carers' Global Impression of Change Scale score measured on a 7-point Likert scale from -3 (very much worse) to +3 (very much improved) Also, adverse events were assessed in each visit ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06101160
Study type Observational [Patient Registry]
Source Cairo University
Contact
Status Completed
Phase
Start date June 30, 2021
Completion date April 30, 2023

See also
  Status Clinical Trial Phase
Completed NCT02425176 - Botulinum Toxin-A for Sialorrhoea Treatment in Asian Adults With Neurological Diseases Phase 2/Phase 3
Completed NCT02610868 - Open-Label and Single-Arm Study of MYOBLOC® in the Treatment of Troublesome Sialorrhea in Adults Phase 3
Active, not recruiting NCT05164367 - Pharmacokinetics of Atropine Oral Gel Early Phase 1
Not yet recruiting NCT05097079 - Efficacy and Safety Study of MYOBLOC® in the Treatment of Sialorrhea in Pediatric Subjects Phase 3
Completed NCT01994109 - Efficacy and Safety Study of MYOBLOC® Followed by Open-Label Multiple-Treatment With MYOBLOC® in the Treatment of Troublesome Sialorrhea in Adult Subjects Phase 3
Active, not recruiting NCT01489904 - Application of Botulinum Toxin Type A in Salivary Glands in the Treatment of Drooling in Patients With Cerebral Palsy Phase 2/Phase 3
Recruiting NCT04873115 - Double-blind, Placebo-controlled, Randomized Clinical Trial Comparing the Efficacy and Safety of Sialanar Plus orAl rehabiLitation Against Placebo Plus Oral Rehabilitation for chIldren and Adolescents With seVere Sialorrhoea and Neurodisabilties, Phase 4
Withdrawn NCT03704168 - Safety and Efficacy of Cryoablation in Management of Sialorrhea in Patients With Neurological Disorders N/A
Completed NCT01653132 - Incobotulinum Toxin A (Xeomin®) for Troublesome Sialorrhea in Parkinson's Disease (PD)/Parkinsonism Phase 2
Completed NCT00491894 - Safety and Efficacy Study of Oral Glycopyrrolate Liquid for the Treatment of Pathologic (Chronic Moderate to Severe) Drooling in Pediatric Patients 3 to 18 Years of Age With Cerebral Palsy or Other Neurologic Conditions Phase 3
Completed NCT04197037 - Prevalence of Sialorrhea in Patients Treated With Clozapine
Completed NCT01191398 - Effectiveness of Atropine and Glycopyrrolate to Reduce Hyper Salivation With Ketamine Sedation N/A
Completed NCT01118143 - Oral Health Literacy Tailored Communication N/A
Recruiting NCT02382198 - Study of Glycopyrrolate for Moderate-to-severe Sialorrhea in Parkinson's Disease Phase 2
Completed NCT00125203 - Study of Myobloc in the Treatment of Sialorrhea (Drooling) in Patients With Amyotrophic Lateral Sclerosis (ALS) Phase 2/Phase 3
Completed NCT02613494 - Clozapine-induced Hypersalivation - Feasibility Trial Phase 1/Phase 2
Not yet recruiting NCT03747536 - Ipratropium Bromide Spray as Treatment for Sialorrhea in Children Phase 2
Completed NCT01551940 - Toxin Treatment for Amyotrophic Lateral Sclerosis (ALS) Related Sialorrhea Phase 2
Completed NCT00683891 - FazaClo Outcomes in the Control of Schizophrenia (FOCUS) Study Survey N/A