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The Use of Tadalafil in Confirmed COVID-19 Pneumonia.

Primary Purpose

COVID, Sars-CoV2, ARDS, Human

Status
Withdrawn
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Tadalafil Pill
Sponsored by
Santa Barbara Cottage Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Hospitalized patients at SBCH with confirmed COVID19 pneumonia (PCR + clinical signs/symptoms of lower respiratory disease)
  • Patients currently on a ventilator
  • Patients who meet the Berlin definition of ARDS
  • Patients who have access to measure a mixed venous oxygen saturation (i.e., patients with an internal jugular central venous catheter)
  • Patient and/or Legally Authorized Representative is willing/able to provide informed consent

Exclusion Criteria:

  • As tadalafil is currently a FDA Class B1 medication, indicating that little information is available, pregnant women along with women who are actively breastfeeding will be excluded from this series.
  • All patients under 18
  • Patients who are routinely taking nitrate medications
  • All patients using Tadalafil daily for pulmonary arterial hypertension (Note: patients using Tadalafil intermittently for erectile dysfunction may still participate in the study)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Tadalafil Group

    Arm Description

    Each patient will be given tadalafil 40 mg one time

    Outcomes

    Primary Outcome Measures

    Improvement in P:F ratio
    Change in a patient's P:F ratio after medication administration
    Improvement in oxygen saturation
    Change in oxyhemoglobin as noted on an arterial blood gas sample after medication administration
    Improvement in partial pressure of oxygen in the bloodstream
    Change in oxygen partial pressure (aka PaO2) as noted on an arterial blood gas sample after medication administration

    Secondary Outcome Measures

    Full Information

    First Posted
    June 28, 2021
    Last Updated
    June 30, 2021
    Sponsor
    Santa Barbara Cottage Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04946162
    Brief Title
    The Use of Tadalafil in Confirmed COVID-19 Pneumonia.
    Official Title
    The Use of Tadalafil in Confirmed COVID-19 Pneumonia.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2021
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    The investigators never completed the IRB application due to decrease in need to conduct the study.
    Study Start Date
    April 20, 2020 (Actual)
    Primary Completion Date
    April 20, 2020 (Actual)
    Study Completion Date
    April 20, 2020 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Santa Barbara Cottage Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Our goal is to assess the effects of Tadalafil in the setting of confirmed COVID-19 pneumonia. In particular we plan to assess its effects on oxygen saturation, P:F ratio, and mixed central venous oxygen We plan to recruit all hospitalized patients at Santa Barbara Cottage Hospital with a confirmed COVID19 pneumonia (positive PCR + clinical signs/symptoms of lower respiratory disease) who meet the Berlin definition of ARDS and have access to measure a mixed venous oxygen saturation. For the purposes of obtaining mixed central venous oxygen, all participating patients will already have an internal jugular central venous catheter in place for inclusion in this study. Since all patients will be intubated, their Legally Authorized Representative (LAR) will be approached to discuss the study and asked to participate in the study by an ICU physician, either the attending physician or a medical resident. Informed consent will be obtained from the LAR by an ICU attending physician or resident involved in the study prior to participation. Patients who meet the above eligibility criteria will have baseline levels of mixed central venous oxygen, oxygen saturation, P:F ratio, blood pressure and PaO2 recorded. Each patient will then receive Tadalafil 40mg once. The above listed parameters will be monitored again 30 minutes after drug administration and 4 hours after drug administration. No other medication or ventilator changes will be made during this time period outside of emergent changes in the setting of patient deterioration. We will continue to analyze the data in the event of emergent ventilator changes.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    COVID, Sars-CoV2, ARDS, Human

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Single Group Assignment
    Model Description
    Participants will serve as a self-control, with values recorded pre-medication, 30 minutes after medication administration, and 4 hours after administration.
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Tadalafil Group
    Arm Type
    Experimental
    Arm Description
    Each patient will be given tadalafil 40 mg one time
    Intervention Type
    Drug
    Intervention Name(s)
    Tadalafil Pill
    Intervention Description
    Each patient will be given tadalafil 40 mg one time
    Primary Outcome Measure Information:
    Title
    Improvement in P:F ratio
    Description
    Change in a patient's P:F ratio after medication administration
    Time Frame
    Pre-medication, 30 minutes post medication, 4 hours post-medication
    Title
    Improvement in oxygen saturation
    Description
    Change in oxyhemoglobin as noted on an arterial blood gas sample after medication administration
    Time Frame
    Pre-medication, 30 minutes post medication, 4 hours post-medication
    Title
    Improvement in partial pressure of oxygen in the bloodstream
    Description
    Change in oxygen partial pressure (aka PaO2) as noted on an arterial blood gas sample after medication administration
    Time Frame
    Pre-medication, 30 minutes post medication, 4 hours post-medication

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Hospitalized patients at SBCH with confirmed COVID19 pneumonia (PCR + clinical signs/symptoms of lower respiratory disease) Patients currently on a ventilator Patients who meet the Berlin definition of ARDS Patients who have access to measure a mixed venous oxygen saturation (i.e., patients with an internal jugular central venous catheter) Patient and/or Legally Authorized Representative is willing/able to provide informed consent Exclusion Criteria: As tadalafil is currently a FDA Class B1 medication, indicating that little information is available, pregnant women along with women who are actively breastfeeding will be excluded from this series. All patients under 18 Patients who are routinely taking nitrate medications All patients using Tadalafil daily for pulmonary arterial hypertension (Note: patients using Tadalafil intermittently for erectile dysfunction may still participate in the study)

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    32381264
    Citation
    Klok FA, Kruip MJHA, van der Meer NJM, Arbous MS, Gommers D, Kant KM, Kaptein FHJ, van Paassen J, Stals MAM, Huisman MV, Endeman H. Confirmation of the high cumulative incidence of thrombotic complications in critically ill ICU patients with COVID-19: An updated analysis. Thromb Res. 2020 Jul;191:148-150. doi: 10.1016/j.thromres.2020.04.041. Epub 2020 Apr 30.
    Results Reference
    background
    PubMed Identifier
    32299776
    Citation
    Magro C, Mulvey JJ, Berlin D, Nuovo G, Salvatore S, Harp J, Baxter-Stoltzfus A, Laurence J. Complement associated microvascular injury and thrombosis in the pathogenesis of severe COVID-19 infection: A report of five cases. Transl Res. 2020 Jun;220:1-13. doi: 10.1016/j.trsl.2020.04.007. Epub 2020 Apr 15.
    Results Reference
    background
    PubMed Identifier
    15234326
    Citation
    Keyaerts E, Vijgen L, Chen L, Maes P, Hedenstierna G, Van Ranst M. Inhibition of SARS-coronavirus infection in vitro by S-nitroso-N-acetylpenicillamine, a nitric oxide donor compound. Int J Infect Dis. 2004 Jul;8(4):223-6. doi: 10.1016/j.ijid.2004.04.012.
    Results Reference
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    PubMed Identifier
    15650225
    Citation
    Akerstrom S, Mousavi-Jazi M, Klingstrom J, Leijon M, Lundkvist A, Mirazimi A. Nitric oxide inhibits the replication cycle of severe acute respiratory syndrome coronavirus. J Virol. 2005 Feb;79(3):1966-9. doi: 10.1128/JVI.79.3.1966-1969.2005.
    Results Reference
    background
    PubMed Identifier
    19470885
    Citation
    Galie N, Brundage BH, Ghofrani HA, Oudiz RJ, Simonneau G, Safdar Z, Shapiro S, White RJ, Chan M, Beardsworth A, Frumkin L, Barst RJ; Pulmonary Arterial Hypertension and Response to Tadalafil (PHIRST) Study Group. Tadalafil therapy for pulmonary arterial hypertension. Circulation. 2009 Jun 9;119(22):2894-903. doi: 10.1161/CIRCULATIONAHA.108.839274. Epub 2009 May 26. Erratum In: Circulation. 2011 Sep 6;124(10):e279. Dosage error in article text.
    Results Reference
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    Links:
    URL
    https://www.globenewswire.com/news-release/2020/03/25/2006042/0/en/Nu-Med-Plus-Closely-Monitoring-Outcomes-on-Two-New-Human-Clinical-Trials-Using-Inhaled-Nitric-Oxide-in-Treatment-of-COVID-19.html
    Description
    Nu-Med Plus Closely Monitoring Outcomes on Two New Human Clinical Trials Using Inhaled Nitric Oxide in Treatment of COVID-19
    URL
    https://clinicaltrials.gov/ct2/show/NCT04304313
    Description
    A Pilot Study of Sildenafil in COVID-19

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    The Use of Tadalafil in Confirmed COVID-19 Pneumonia.

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