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Nebulized Fentanyl for Respiratory Symptoms in Patients With COVID-19 (Ventanyl)

Primary Purpose

COVID-19 Pneumonia

Status
Not yet recruiting
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Nebulized Fentanyl
Sponsored by
Hamad Medical Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID-19 Pneumonia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age: 18 - 65 years
  • Confirmed diagnosis (COVID-19) - positive PCR
  • Tachypnoea (Respiratory rate> 30/min)
  • Ability to provide informed consent and perform all study procedures

Exclusion Criteria:

  • History of allergy or adverse reaction to fentanyl or other opioids
  • Pregnancy
  • Active neuromuscular or musculoskeletal disease.
  • Active malignancy
  • Morbid obesity (Body mass index >40)
  • Use of opioids in the previous 4 weeks.
  • Inability to provide informed consent and perform all study procedures.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Placebo Comparator

    Arm Label

    Nebulized Fentanyl

    Nebulized 0.9% Saline Solution

    Arm Description

    Intervention group (n=100): Administration of nebulized Fentanyl (25 μg in 5 ml of normal saline) over 15 mins, thrice daily using a traditional nebulizer. Treatment duration - 48 hours

    Control group (n=100): Administration of nebulized 0.9% saline solution (5 ml of normal saline), over 15 minutes, thrice daily using a traditional nebulizer. Treatment duration - 48 hours

    Outcomes

    Primary Outcome Measures

    Breathlessness
    The severity of breathlessness will be measured by the 10-point Borg Scale. Patients will be instructed to use this scale to rate the difficulty of breathing. It starts at number 0 where breathing is causing no difficulty at all and progresses through to number 10 where breathing difficulty is maximal.
    Throat Pain
    Throat pain will be graded by the Numerical Rating Scale (NRS), in which patients will be asked to circle the number between 0 and 10, that fits best to their pain intensity. Zero usually represents 'no pain at all' whereas the upper limit represents 'the worst pain ever possible'.
    Cough
    The cough severity score represents a simple instrument, using a 10 point scale, where the patient can indicate the severity of their cough between the two extremes: one for no cough while 100 mm is the most severe cough.

    Secondary Outcome Measures

    Full Information

    First Posted
    December 20, 2021
    Last Updated
    December 27, 2021
    Sponsor
    Hamad Medical Corporation
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05165992
    Brief Title
    Nebulized Fentanyl for Respiratory Symptoms in Patients With COVID-19
    Acronym
    Ventanyl
    Official Title
    Nebulized Fentanyl for Respiratory Symptoms in Patients With COVID-19 (Ventanyl Trial)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2021
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    February 2022 (Anticipated)
    Primary Completion Date
    November 2022 (Anticipated)
    Study Completion Date
    December 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Hamad Medical Corporation

    4. Oversight

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

    5. Study Description

    Brief Summary
    Patients with Coronavirus Disease (COVID-19) experience distressing and challenging to manage respiratory symptoms. Interventions such as Oxygen (O2) therapy, oral opiates, and traditional nebulizers like ipratropium bromide and salbutamol, are variably effective, and therapeutic responses in individual patients are difficult to predict. The purpose of this study is to investigate the efficacy of nebulized fentanyl citrate on dyspnea, cough, and throat pain in patients with COVID-19, as well as evaluate the safety with any potential adverse events. In COVID-19, about 59% of patients will exhibit cough, 35% generalized body ache and sore throat and 31% will have dyspnea. Nebulized Lidocaine, magnesium, and opioids are alternative methods for the management of respiratory symptoms in various patients. Fentanyl nebulization was found to be effective in decreasing dyspnea in chronic obstructive pulmonary disease (COPD) patients by decreasing the rate of spontaneous respiratory rate, modulating cortical activity, and diminishing the brain stem chemoreceptor response to hypoxia and hypercarbia. The investigators hypothesize that nebulized fentanyl is superior to nebulized saline in suppressing cough, respiratory drive, improving breathlessness or dyspnea with the additional advantage of throat pain relief with minimal adverse effects in patients with COVID-19.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    COVID-19 Pneumonia

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    200 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Nebulized Fentanyl
    Arm Type
    Active Comparator
    Arm Description
    Intervention group (n=100): Administration of nebulized Fentanyl (25 μg in 5 ml of normal saline) over 15 mins, thrice daily using a traditional nebulizer. Treatment duration - 48 hours
    Arm Title
    Nebulized 0.9% Saline Solution
    Arm Type
    Placebo Comparator
    Arm Description
    Control group (n=100): Administration of nebulized 0.9% saline solution (5 ml of normal saline), over 15 minutes, thrice daily using a traditional nebulizer. Treatment duration - 48 hours
    Intervention Type
    Drug
    Intervention Name(s)
    Nebulized Fentanyl
    Intervention Description
    Administration of nebulized Fentanyl (25 μg in 5 ml of normal saline) over 15 mins, thrice daily using a traditional nebulizer. Treatment duration - 48 hours
    Primary Outcome Measure Information:
    Title
    Breathlessness
    Description
    The severity of breathlessness will be measured by the 10-point Borg Scale. Patients will be instructed to use this scale to rate the difficulty of breathing. It starts at number 0 where breathing is causing no difficulty at all and progresses through to number 10 where breathing difficulty is maximal.
    Time Frame
    15-minutes post-treatment
    Title
    Throat Pain
    Description
    Throat pain will be graded by the Numerical Rating Scale (NRS), in which patients will be asked to circle the number between 0 and 10, that fits best to their pain intensity. Zero usually represents 'no pain at all' whereas the upper limit represents 'the worst pain ever possible'.
    Time Frame
    15-minutes post-treatment
    Title
    Cough
    Description
    The cough severity score represents a simple instrument, using a 10 point scale, where the patient can indicate the severity of their cough between the two extremes: one for no cough while 100 mm is the most severe cough.
    Time Frame
    15-minutes post-treatment

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age: 18 - 65 years Confirmed diagnosis (COVID-19) - positive PCR Tachypnoea (Respiratory rate> 30/min) Ability to provide informed consent and perform all study procedures Exclusion Criteria: History of allergy or adverse reaction to fentanyl or other opioids Pregnancy Active neuromuscular or musculoskeletal disease. Active malignancy Morbid obesity (Body mass index >40) Use of opioids in the previous 4 weeks. Inability to provide informed consent and perform all study procedures.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Abdulqadir J Nashwan
    Phone
    0097466473549
    Email
    ANashwan@hamad.qa
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Mohamad Y Khatib, MD
    Organizational Affiliation
    Hamad Medical Corporation
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided
    Citations:
    PubMed Identifier
    33145156
    Citation
    Hildreth L, Pett D, Higgins E. Nebulized fentanyl for refractory dyspnea secondary to chronic obstructive pulmonary disease (COPD): A case report. Respir Med Case Rep. 2020 Oct 12;31:101251. doi: 10.1016/j.rmcr.2020.101251. eCollection 2020.
    Results Reference
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    PubMed Identifier
    14769753
    Citation
    Foral PA, Malesker MA, Huerta G, Hilleman DE. Nebulized opioids use in COPD. Chest. 2004 Feb;125(2):691-4. doi: 10.1378/chest.125.2.691.
    Results Reference
    background
    PubMed Identifier
    28687551
    Citation
    Afolabi TM, Nahata MC, Pai V. Nebulized opioids for the palliation of dyspnea in terminally ill patients. Am J Health Syst Pharm. 2017 Jul 15;74(14):1053-1061. doi: 10.2146/ajhp150893.
    Results Reference
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    PubMed Identifier
    25010531
    Citation
    Krajnik M, Jassem E, Sobanski P. Opioid receptor bronchial tree: current science. Curr Opin Support Palliat Care. 2014 Sep;8(3):191-9. doi: 10.1097/SPC.0000000000000072.
    Results Reference
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    PubMed Identifier
    24914770
    Citation
    Boyden JY, Connor SR, Otolorin L, Nathan SD, Fine PG, Davis MS, Muir JC. Nebulized medications for the treatment of dyspnea: a literature review. J Aerosol Med Pulm Drug Deliv. 2015 Feb;28(1):1-19. doi: 10.1089/jamp.2014.1136. Epub 2014 Jun 10.
    Results Reference
    background
    PubMed Identifier
    18443635
    Citation
    Benyamin R, Trescot AM, Datta S, Buenaventura R, Adlaka R, Sehgal N, Glaser SE, Vallejo R. Opioid complications and side effects. Pain Physician. 2008 Mar;11(2 Suppl):S105-20.
    Results Reference
    background
    PubMed Identifier
    18046866
    Citation
    Uronis HE, Currow DC, Abernethy AP. Palliative management of refractory dyspnea in COPD. Int J Chron Obstruct Pulmon Dis. 2006;1(3):289-304. doi: 10.2147/copd.2006.1.3.289.
    Results Reference
    background
    PubMed Identifier
    34582457
    Citation
    Elliott J, Whitaker M, Bodinier B, Eales O, Riley S, Ward H, Cooke G, Darzi A, Chadeau-Hyam M, Elliott P. Predictive symptoms for COVID-19 in the community: REACT-1 study of over 1 million people. PLoS Med. 2021 Sep 28;18(9):e1003777. doi: 10.1371/journal.pmed.1003777. eCollection 2021 Sep.
    Results Reference
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    PubMed Identifier
    33170317
    Citation
    Scialo F, Daniele A, Amato F, Pastore L, Matera MG, Cazzola M, Castaldo G, Bianco A. ACE2: The Major Cell Entry Receptor for SARS-CoV-2. Lung. 2020 Dec;198(6):867-877. doi: 10.1007/s00408-020-00408-4. Epub 2020 Nov 10.
    Results Reference
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    Nebulized Fentanyl for Respiratory Symptoms in Patients With COVID-19

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