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Recruiting NCT06429982

Dexamethasone Use in Pediatric Rhabdomyolysis Patients in Addition to Standard Protocols

Phase I Interventional Rhabdomyolysis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Dexamethasone, Placebo.
Who it may be relevant to
Registry conditions: Rhabdomyolysis. Basic parameters: 6 months — 25 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Clinical Trial to Assess Whether Dexamethasone Addition to Standard Protocols for Non-Traumatic Rhabdomyolysis of Unknown or Genetic Etiologies Improves Patient Outcomes

Overview

There is a significant unmet need for optimized treatment in rhabdomyolysis. There are few prospective interventional studies on treatment for rhabdomyolysis, a condition which affects diverse and underrepresented populations at a higher rate. While steroids are often used off-label, a systematic study has not yet been initiated, and steroids have not been yet considered in as a consideration to standard care guidelines. The hypothesis is that patients who receive dexamethasone in addition to standard care versus placebo and standard care will have improvement in pain, length of hospital stay, and decrease in kidney complications.

Detailed description

Study Objective:

This is a single center, 2-year, blinded prospective randomized study for those diagnosed with rhabdomyolysis age six months-25 years using dexamethasone versus placebo treatment in addition to standard care in up to 50 patients.

Study Design:

Patients will be enrolled with a 2:1 ratio of treatment of dexamethasone for 5 days versus placebo treatment for 5 days in addition to receiving standard care. The treatment period for each subject will be five days treatment with oral treatment once per day with study drug (dexamethasone versus placebo). All patients will also receive standard care. Patients and their parent/ caregiver will have the option to complete surveys before and after treatment in order to assess pain level and treatment improvement. Chart review will be performed on all patients throughout and after the five-day study treatment period. There will be no additional interventions.

Interventions

  • Drug Dexamethasone
    Steroid five day treatment
  • Drug Placebo
    Placebo control group

Primary outcome measures

  • Length of Stay [Time frame: Primarily 5 days - 1 year]
  • Muscle breakdown [Time frame: Primarily 5 days - 1 year]
  • Renal complications [Time frame: Primarily 5 days - 1 year]
Secondary outcome measures (1)
  • Quantitative Pain Outcomes [Time frame: 14 days]

Eligibility criteria

Inclusion criteria

  • Diagnosis of rhabdomyolysis defined as creatine kinase> 5000 with trauma excluded
  • Ability of parents/patients to understand and the willingness to sign a written informed consent document.
  • Patients ages 12 and older will sign written assent

Exclusion criteria

  • Already taking systemic steroids.
  • Inability to comply with study instructions.
  • Uncontrolled intercurrent illness or psychiatric illness/social situations that would limit compliance with study requirements.
  • Pregnant women.

o A urine pregnancy test will be performed for women of child-bearing potential.

  • Below gestational age of 40 weeks
  • Allergy to fluconazole, clotrimazole or nystatin.
  • Cannot tolerate PO medications

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Quadruple blind
Primary purpose
Treatment

Study locations

United States · 1 center
  • Childrens National — Washington D.C.

Publications

  • Chavez LO, Leon M, Einav S, Varon J. Beyond muscle destruction: a systematic review of rhabdomyolysis for clinical practice. Crit Care. 2016 Jun 15;20(1):135. doi: 10.1186/s13054-016-1314-5. PMID 27301374
  • Summerlin ML, Regier DS, Fraser JL, Chapman KA, Kafashzadeh D, Billington C Jr, Kisling M, Grochowsky A, Ah Mew N, Shur N. Use of dexamethasone in idiopathic, acute pediatric rhabdomyolysis. Am J Med Genet A. 2021 Feb;185(2):500-507. doi: 10.1002/ajmg.a.62000. Epub 2020 Dec 10. PMID 33300687
  • Szugye HS. Pediatric Rhabdomyolysis. Pediatr Rev. 2020 Jun;41(6):265-275. doi: 10.1542/pir.2018-0300. PMID 32482689

Identifiers

NCT: NCT06429982 · STUDY00000710

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗