An interventional study of Rosuvastatin (crestor) and Placebo in Acute Respiratory Distress Syndrome, Influenza and H1N1 Influenza, sponsored by Gordon Bernard. Terminated at 21 sites in United States. Open to participants aged 13 Years and older. Per ClinicalTrials.gov, last updated 2017-03-22.
Sponsored by Gordon Bernard · Not applicable, Interventional, and Treatment
To assess the efficacy and safety of oral rosuvastatin in patients with suspected or confirmed influenza who require intensive care unit (ICU) admission due to respiratory distress.
Hypothesis: Rosuvastatin therapy will improve mortality and reduce the need for mechanical ventilation in patients experiencing respiratory distress as a complication of influenza.
2,214 studies on the registry are indexed under Influenza, Human; 164 are open to participants now.
This study's enrollment of 7 is below the median of 238 across 1,853 interventional studies indexed under Influenza, Human.
Browse Influenza, Human studies →Gordon Bernard is the lead sponsor of 2 studies on the registry; none are open to participants now.
Counted across the registry records on this site, refreshed daily.
Requirement for ICU (or ICU step-down) admission due to respiratory distress defined as:
Participants must receive the first dose of study drug within 48 hours following ICU admission for confirmed or suspected influenza or be excluded from participation in the study.
Exclusion Criteria:
Placebo
Drug: Placebo
Experimental arm
Drug: Rosuvastatin (crestor)
20 mg tablets once daily x max 28 days or for an additional 3 days following ICU discharge
Also known as: Crestor
Placebo tablet identical to active therapy. 1 tablet per day
Also known as: Placebo, sugar pill
Hospital Mortality to Day 28 or if Mortality is Not Different Between Groups, Time to Achieve Resolution of Respiratory Failure (e.g., Time to Unassisted Breathing in Survivors (Including Patient's Never Requiring Mechanical Ventilation).
No outcome analyses were run as the sample size was not of sufficient size for a comparison with only 7 of \>2000 participants planned/anticipated actually enrolled.
Time frame: 28 days
Study terminated due to lack of recruitment due to earlier than anticipated end to H1N1 flu season
| Milestone | Placebo Tablet | Rosuvastatin (Crestor) |
|---|---|---|
| Started | 4 | 3 |
| Completed | 4 | 3 |
| Not completed | 0 | 0 |
No outcome analyses were run as the sample size was not of sufficient size for a comparison with only 7 of \>2000 participants planned/anticipated actually enrolled.
No measurements were reported for this outcome.
Collected over 28 days. Non-serious events are listed at a 5% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Placebo Tablet | — | 0/4 (0%) | 1/4 (25%) |
| Rosuvastatin (Crestor) | — | 0/3 (0%) | 0/3 (0%) |
| Event | Placebo Tablet | Rosuvastatin (Crestor) |
|---|---|---|
| Increased liver enzymes-AST/ALTHepatobiliary disorders | 1/4 | 0/3 |
| Age, Categorical(Participants) | Placebo Tablet | Rosuvastatin (Crestor) | Total |
|---|---|---|---|
| <=18 years | 0 | 0 | 0 |
| Between 18 and 65 years | 4 | 3 | 7 |
| >=65 years | 0 | 0 | 0 |
| Age, Continuous(years) | Placebo Tablet | Rosuvastatin (Crestor) | Total |
|---|---|---|---|
| Mean | 43.03 ± 12.89 | 39.88 ± 5.32 | 41.68 ± 9.76 |
| Sex: Female, Male(Participants) | Placebo Tablet | Rosuvastatin (Crestor) | Total |
|---|---|---|---|
| Female | 1 | 1 | 2 |
| Male | 3 | 2 | 5 |
| Region of Enrollment(participants) | Placebo Tablet | Rosuvastatin (Crestor) | Total |
|---|---|---|---|
| United States | 4 | 3 | 7 |
This study is terminated, as verified in Jun 2013. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
Gordon Bernard