Perfused blood volume will be measured by CT scan at two time points and compared at two points, pre and post the administration of sildenafil.
| Group | Value | 95% CI |
|---|---|---|
| Nonsusceptible Smokers (NS) | 0.37 | ± 0.03 |
| Susceptible Smoker (SS) | 0.42 | ± 0.09 |
Last reviewed · How we verify
Hypoxic Pulmonary Vasoconstriction Pilot Study
Phase 4 trial testing Sildenafil study group in Emphysema in 22 participants. Completed in 13 January 2014.
| Lead sponsor | Eric A. Hoffman |
|---|---|
| Phase | Phase 4 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | single group |
| Masking | none |
| Primary purpose | basic science |
| Enrollment | 22 |
| Start date | 29 June 2011 |
| Primary completion | 13 January 2014 |
| Estimated completion | 13 January 2014 |
| Sites | 1 location across United States |
Eric A. Hoffman — full company profile →
Adults 30 to 60, any sex, with Emphysema. Patients with the condition only — healthy volunteers not accepted.
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Perfused blood volume will be measured by CT scan at two time points and compared at two points, pre and post the administration of sildenafil.
| Group | Value | 95% CI |
|---|---|---|
| Nonsusceptible Smokers (NS) | 0.37 | ± 0.03 |
| Susceptible Smoker (SS) | 0.42 | ± 0.09 |
The purpose of this study is to determine if the events leading to smoking-associated centrilobular and paraseptal emphysema are caused by a failure of the lungs' inherent mechanisms to block hypoxic pulmonary vasoconstriction (HPV) in areas of smoking-induced inflammation.
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
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