Exhaled Carbon Monoxide as a Marker of Hemolysis in Sickle Cell Disease- an Exploratory Study
Withdrawn before enrolling
Conditions studied: Sickle Cell Disease
In brief
The investigators propose to evaluate etCO in patients with HbSS, HbSC, and HbS-beta thalassemia during routine clinic visits, and longitudinally. Our goal is to know whether etCO differs amongst subjects with different sickle cell syndrome genotypes, and whether it is a stable marker of hemolytic rate, as reflected in routine labs obtained for clinical care (including total hemoglobin, reticulocyte count, lactate dehydrogenase, and, when sampled, total and direct bilirubin). We hope to establish whether this inexpensive and non-invasive test faithfully reflects hemolytic parameters in sickle cell syndromes.
Key facts
- Study ID
- NCT01888614
- Run by
- University Hospitals Cleveland Medical Center
- People needed
- 0
- Starts
- 2013-06-01
- Expected to finish
- 2016-12-01
- Last updated by the study team
- 2016-12-23
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- All adult sickle patients presenting for follow up at the outpatient sickle cell clinic who are capable of following simple instructions.
You may not qualify if…
- A recent (2 week) history of lung infection, asthma, acute chest syndrome, or COPD exacerbation and/or a significant pulmonary dysfunction in the recent (3-6 month) past.
Where it is running
- Seidman Cancer Center, University Hospitals — Cleveland, Ohio, United States
Full record on ClinicalTrials.gov
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