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Phase 2 N=54 Randomized Quadruple-blind Treatment

Inhaled Mometasone to Reduce Painful Episodes in Patients With Sickle Cell Disease

Sickle Cell Disease

Enrolled (actual)
54
Serious AEs
0.0%
Results posted
Mar 2019
Primary outcome: Primary: Number of Participants Who Completed Follow up — 35; 17 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Mometasone Furoate (Drug); Placebo (Drug)
Age
Pediatric, Adult, Older Adult · 15+ yrs
Sex
All
Sponsor
Jeffrey Glassberg
Primary completion
Nov 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants Who Completed Follow up
35; 17
SECONDARY
Change in Exhaled Nitric Oxide (eNO)
0.63; 2.71
SECONDARY
Change in Soluble Vascular Cell Adhesion Molecule (sVCAM) Level
-182.47; 170.25
SECONDARY
Change in Adult Sickle Cell Quality of Life Measurement Information System (ASCQ-Me)
2.8; 6.9
SECONDARY
The Medication Adherence Report Scale
17.7; 17.1
SECONDARY
Change in the Numerical Rating Scale (NRS) for Pain
2.09; 2.82
SECONDARY
Asthma Control Test
17.7; 17.1
SECONDARY
Admissions or Visits to the Hospital
0.97; 1.12; 0.37; 0.59; 0.37; 0.47
SECONDARY
Change in Reticulocytes Count
-0.15; 0.07
SECONDARY
Change in FEV1/FVC
-0.71; -1.41

Summary

The proposed research is designed to test the global hypothesis that inhaled corticosteroids (ICS), a therapy developed to treat asthma, will prevent vasoocclusive painful episodes in adults with Sickle Cell Disease (SCD) who wheeze, but do not meet criteria for a diagnosis of asthma. The specific aims of this proposal are 1) Conduct a feasibility study - a randomized controlled trial of ICS for adults with SCD who do not meet criteria for a diagnosis of asthma but report recurrent cough or wheezing, 2) Measure the effects of ICS on biological correlates of pulmonary inflammation (as determined by exhaled nitric oxide) and vascular injury (as determined by sVCAM) in SCD, and 3) Compare properties of traditional and Bayesian adaptive clinical trial design for therapeutic trials in SCD in preparation for designing a definitive trial of ICS. These aims have the potential to 1) change the standard of care for individuals with SCD and recurrent cough or wheeze, 2) provide insight into the pathogenesis of non-asthmatic wheezing in SCD and its response to treatment, 3) explore the suitability of innovative clinical trial designs to overcome the challenges that have hindered therapeutic innovation for SCD.

Eligibility Criteria

Inclusion Criteria

  • Age 15 or older
  • Sever SCD phenotypes (Hb SS and Sβthalassemia0)
  • A positive response to cough/wheeze questions

Exclusion Criteria

  • Patient carries a physician diagnosis of asthma
  • Patient is prescribed asthma medications
  • Patient is currently having a painful crisis (as defined by validated pain diary questions)
  • Patient has acute respiratory symptoms
  • Known hypersensitivity to milk proteins
  • Meets criteria for our operational diagnosis of asthma
  • More than 15 ED visits for pain over the preceding 12 months
  • Admitted or discharged from the hospital for SCD pain within the last 7 days
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02061202). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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