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TREAT-SC: Early, Short Course Oral Dexamethasone for the Treatment of Sydenham Chorea in Children

Phase 3
Not yet recruiting
Conditions
Rheumatic Fever
Sydenham Chorea
Interventions
Registration Number
NCT06259006
Lead Sponsor
Starship Child Health, Te Toka Tumai Auckland
Brief Summary

The purpose of this study is to find out whether an early three-day course of an oral steroid medication (dexamethasone) can improve the physical and mental recovery and wellbeing for children with Sydenham's chorea.

Sydenham's chorea is a condition that impacts approximately 12% of children with acute rheumatic fever. It is caused by inflammation in the brain following an abnormal immune response to Group A streptococcus bacterial infection. Sydenham's chorea is a movement disorder that causes children's faces, hands, and feet to move quickly and uncontrollably, and can also affect mood and concentration. The physical recovery from Sydenham's chorea can take two to six months but the mental recovery (e.g. mood and concentration) can take longer to resolve. Sydenham's chorea remains endemic in Māori, Pacific Islander, Aboriginal and Torres Strait Islander children in New Zealand and Australia.

There is limited evidence to direct treatment of Sydenham's chorea, and clinical practice differs widely around the world. Dexamethasone is an oral steroid which targets the abnormal immune response and successfully treats other immune-mediated brain disorders, with good tolerability.

TREAT-SC is a randomized, double-blinded, placebo-controlled trial which will investigate whether a three day course of oral dexamethasone safely and effectively treats the movement disorder and psychiatric symptoms of Sydenham's chorea. The trial will recruit 80 participants from study sites in Australia and New Zealand.

Detailed Description

Aim: The aim of the trial is to determine whether an early, short course of oral dexamethasone is a safe and effective treatment to reduce morbidity associated with Sydenham's chorea in New Zealand and Australian children.

Objectives:

* The primary objective is to determine whether oral dexamethasone is an effective treatment to reduce Sydenham's chorea severity in New Zealand and Australian children at one month

* The secondary objectives are to determine whether oral dexamethasone is an effective treatment to reduce Sydenham's chorea severity at different time points, relapse and recurrence rates at three and 12 months, total hospital length of stay at three months, treatment failure at 14 days, use of adjunctive chorea treatments, Universidade Federal de Minas Gerais (UFMG) Sydenham's Chorea Rating Scale (USCRS) subscores, and psychiatric symptoms scored by the Strengths and Difficulties Questionnaire at one, three and 12 months. The safety of oral dexamethasone use will be assessed at study visits on days three and seven and at one month to monitor for any adverse events which may relate to dexamethasone use.

Research Design: TREAT-SC is a pragmatic parallel-group, double-blinded, placebo-controlled, 1:1 randomized efficacy trial comparing a three-day course of oral dexamethasone with placebo to treat Sydenham's chorea in New Zealand and Australian children. TREAT-SC will be a multi-site trial with participants recruited from hospitals in New Zealand and Australia.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
80
Inclusion Criteria
  1. Sydenham's chorea of any severity diagnosed by a paediatrician or neurologist based on national ARF guidelines
  2. Child or adolescents aged 4 years to <18 years of age
Exclusion Criteria
  1. Administered steroids or intravenous immunoglobulin since onset of the current Sydenham's chorea episode
  2. Evidence of concomitant severe, acute infection
  3. History of hypersensitivity to dexamethasone or its excipients
  4. Pregnancy
  5. Confirmed exposure of an unimmunised child to measles, mumps, rubella or chickenpox within the previous four weeks
  6. Receipt of a live vaccine within the previous four weeks
  7. Medical condition or treatment with medication which in the opinion of the trial investigators would make the child unsuitable for the trial

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
DexamethasoneDexamethasone OralParticipants will receive oral dexamethasone 20mg/m2/day in three divided doses, (maximum dose 24mg/day), for 3 days
Placebo controlPlaceboParticipants will receive oral placebo tablet three times a day for 3 days
Primary Outcome Measures
NameTimeMethod
Chorea severity at 1 month1 month

Chorea severity measured using the Universidade Federal de Minas Gerais Sydenham's Chorea Rating Scale. Scores range from 0 to 108. A higher score correlates with a worse outcome.

Secondary Outcome Measures
NameTimeMethod
Treatment failure at 14 days14 days

Number of participants with treatment failure at 14 days

Universidade Federal de Minas Gerais Sydenham's Chorea Rating Scale Subscores.7 days, 1 month, 3 months, 12 months

Behaviour (0 to 24 points), Activities of Daily Living (0 to 28 points) and Motor Assessment (0-56 points). A higher score correlates with a worse outcome.

Chorea severity7 days, 3 months, 12 months

Chorea severity measured using the Universidade Federal de Minas Gerais Sydenham's Chorea Rating Scale. Scores range from 0 to 108. A higher score correlates with a worse outcome.

Chorea relapse and recurrence3 and 12 months

Number of participants with chorea relapse and recurrence at 3 and 12 months

Psychiatric symptoms1 month, 3 months and 12 months

Strength and Difficulties Questionnaire Total Difficulties Score. The resultant score ranges from 0 to 40. An abnormally high total difficulties score correlates with worse outcome.

Total hospital length of stay3 months

Total hospital length of stay for chorea at three months

Adverse events3 days, 7 days, 1 month

Frequency of adverse events

Use of adjunctive chorea treatments1 month

Number of participants treated with adjunctive chorea treatments

Trial Locations

Locations (2)

Starship Child Health, Te Toka Tumai Auckland, Te Whatu Ora Health New Zealand

🇳🇿

Auckland, New Zealand

Royal Darwin Hospital

🇦🇺

Darwin, Northern Territories, Australia

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