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Withdrawn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
About this trial
This is an interventional treatment trial for COVID
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)
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
NCT ID
NCT04946162
First Posted
June 28, 2021
Last Updated
June 30, 2021
Sponsor
Santa Barbara Cottage Hospital
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Withdrawn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
background
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
background
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
Learn more about this trial
The Use of Tadalafil in Confirmed COVID-19 Pneumonia.
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