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TerminatedNCT00970606STIPUpdated Mar 22, 2017Results posted

STIP: Statin Trial for Influenza Patients

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

Why this study was terminated
Inability to recruit participants since H1N1 epidemic resolved.
Phase
Not applicable
Study type
Interventional
Enrollment
7
Allocation
Randomized
Ages
13 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

Hypothesis: Rosuvastatin therapy will improve mortality and reduce the need for mechanical ventilation in patients experiencing respiratory distress as a complication of influenza.

02

Conditions studied

  • Acute Respiratory Distress Syndrome
  • Influenza
  • H1N1 Influenza

Keywords

  • ARDS
  • H1N1
  • Influenza
  • Statin
03

In context

Influenza, Human

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
13 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Patients with suspected or confirmed influenza (Appendix A)
  2. Requirement for ICU (or ICU step-down) admission due to respiratory distress defined as:

    • SaO2/FiO2 \< 315 or PaO2/FiO2 \< 300
    • Multiply by PB/760 (when altitude exceeds 51000 ft)
    • For FiO2 for non-intubated patients see Appendix B

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

Exclusion Criteria:

  1. No consent/inability to obtain consent
  2. Age less than 13 years
  3. Weight less than 40 kg
  4. Unable to receive or unlikely to absorb enteral study drug (e.g. patients with partial or complete mechanical bowel obstruction, intestinal ischemia, infarction, and short bowel syndrome)
  5. Allergy or intolerance to statins*
  6. Pregnancy or breast feeding
  7. Receiving niacin, fenofibrate, cyclosporine, gemfibrozil, or any antiviral protease inhibitor including but not limited to lopinavir and ritonavir.
  8. Existing clinically significant myositis or myopathy or has a measured CK greater than 5,000 U/L
  9. Requiring statin for underlying disease as determined by the patients attending physician team**.
  10. Severe chronic liver disease (Child-Pugh Score 11-15)
  11. Previous myocardial infarction or thrombotic stroke within the past 6 months 11.12. Any significant funding in the patient's medical history or physical or psychiatric exam prior to randomization that, in the opinion of the investigator, would affect patient safety or compliance or ability to deliver the study drug according to protocol
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Care provider, Investigator, Outcomes assessor)
Enrollment
7 participants (actual)

Study arms

  • Placebo comparator
    Placebo tablet

    Placebo

    Drug: Placebo

  • Experimental
    Rosuvastatin (crestor)

    Experimental arm

    Drug: Rosuvastatin (crestor)

Interventions

  • DrugRosuvastatin (crestor)

    20 mg tablets once daily x max 28 days or for an additional 3 days following ICU discharge

    Also known as: Crestor

  • DrugPlacebo

    Placebo tablet identical to active therapy. 1 tablet per day

    Also known as: Placebo, sugar pill

06

What researchers measure

Primary outcomes

  1. 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

07

Results

Posted Apr 24, 2013
Limitations and caveats
Only able to enroll only 7 participants of \>2000 planned/anticipated, leading to early termination of the study and therefore unable to perform statistical analysis with such a small sample size.

Participant flow

Study terminated due to lack of recruitment due to earlier than anticipated end to H1N1 flu season

Participant flow — Overall Study
MilestonePlacebo TabletRosuvastatin (Crestor)
Started43
Completed43
Not completed00

Outcome measures

PrimaryHospital 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

No measurements were reported for this outcome.

Adverse events

Collected over 28 days. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Placebo Tablet—0/4 (0%)1/4 (25%)
Rosuvastatin (Crestor)—0/3 (0%)0/3 (0%)
Most frequent other events
Most frequent other events
EventPlacebo TabletRosuvastatin (Crestor)
Increased liver enzymes-AST/ALTHepatobiliary disorders1/40/3

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Placebo TabletRosuvastatin (Crestor)Total
<=18 years000
Between 18 and 65 years437
>=65 years000
Age, Continuous
Age, Continuous(years)Placebo TabletRosuvastatin (Crestor)Total
Mean43.03 ± 12.8939.88 ± 5.3241.68 ± 9.76
Sex: Female, Male
Sex: Female, Male(Participants)Placebo TabletRosuvastatin (Crestor)Total
Female112
Male325
Region of Enrollment
Region of Enrollment(participants)Placebo TabletRosuvastatin (Crestor)Total
United States437
08

Study locations

21 sites
  • University of Arkansas
    Little Rock, Alaska, United States
  • Maricopa Integrated Health System
    Phoenix, Arizona, United States
  • Stanford
    Stanford, California, United States
  • Northwestern University
    Chicago, Illinois, United States
  • University of Iowa
    Iowa City, Iowa, United States
  • Johns Hopkins Hospital
    Baltiomore, Maryland, United States
  • Boston University
    Boston, Massachusetts, United States
  • Baystate Medical Center
    Springfiled, Massachusetts, United States
  • Columbia University
    New York, New York, United States
  • Mt Sinai
    New York, New York, United States
  • Moses H. Cone Memorial Hospital
    Greensboro, North Carolina 27401, United States
  • Metro Health
    Cleveland, Ohio, United States
  • Ohio State University
    Columbus, Ohio, United States
  • University of Oregon
    Portland, Oregon, United States
  • University of Pittsburgh
    Pittsburgh, Pennsylvania, United States
  • Medical University of South Carolina
    Charleston, South Carolina, United States
  • Erlanger
    Chattanooga, Tennessee, United States
  • Vanderbilt University
    Nashville, Tennessee 37232, United States
  • University of Texas
    San Antonio, Texas, United States
  • Intermountain
    Murray, Utah, United States
  • University of Virginia
    Charlottesville, Virginia, United States
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 22, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00970606
Lead sponsor
Gordon Bernard
Responsible party
Gordon Bernard (Professor of Medicine, Vanderbilt University Medical Center) — Sponsor-investigator
First posted
Sep 2, 2009
Start date
Oct 2009
Primary completion
Jul 2011
Completion
Jul 2011
Results posted
Apr 24, 2013
Last update
Mar 22, 2017

Study contacts

Gordon R Bernard, M.D.
principal investigator · Vanderbilt University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Jun 2013. You cannot join it, but the record below documents what was studied.

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