Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06429982

Dexamethasone Use in Pediatric Rhabdomyolysis Patients in Addition to Standard Protocols

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

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Children's National Research Institute · Academic / Other
Sex
All
Age
6 Months – 25 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DRUGDexamethasoneSteroid five day treatment
DRUGPlaceboPlacebo control group

Timeline

Start date
2024-10-01
Primary completion
2025-12-01
Completion
2026-12-31
First posted
2024-05-28
Last updated
2025-07-03

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06429982. Inclusion in this directory is not an endorsement.