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Micronized and Ultramicronized Palmitoylethanolamide in COVID-19 Patients

Primary Purpose

Covid19

Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Micronized and ultra-micronized Palmitoylethanolamide (mPEA and umPEA, 300mg + 600mg) oral suspension
Standard Therapy
Sponsored by
Epitech Group SpA
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Covid19

Eligibility Criteria

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

Inclusion Criteria:

  • Intensive Care Unit Hospitalization for interstitial pneumonia due to COVID-19 diagnosis (nasal swab/sputum/bronchoalveolar lavage positive for Sars-Cov-2 infection)

Exclusion Criteria:

  • Pregnancy or breastfeeding;
  • Known allergy or hypersensitivity to the product or its excipients;
  • Inability to take the product per os or via nasogastric tube.

Sites / Locations

  • Anestesia e Rianimazione Azienda Ospedaliera Universitaria Sant'Andrea

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Other

Arm Label

PEA Group

Control Group

Arm Description

Normast® MPS (mPEA and umPEA 300mg + 600mg) oral suspension: 2700mg/die in 3 doses for 28 days, in add-on to standard therapy

Standard therapy only

Outcomes

Primary Outcome Measures

Number of responder participants after 7 days of treatment
Responder: decrease ≥ 30% from baseline of IL-6 blood levels

Secondary Outcome Measures

Change of pro-inflammatory markers (IL-6, IL-1 alpha, IL-1 beta, TNF-alpha, PCR, PCT, neopterin)
Change of anti-inflammatory markers (IL-4, IL-10)
Change of brain damage markers (S100b, ENS)
Change of coagulation indices (INR, fibrinogen, D-dimer)
Change of hematological parameters
leukocyte formula (lymphocytes, CD4 / CD8 ratio)
Change of oxygenation indices (P/F ratio, lactates)
Number of participants who developed delirium
Confusion Assessment Method-Intensive Care Unit (CAM-ICU) (0-1: no delirium; >1 delirium)
Number of participants who developed anxiety and/or depression
Hospital Anxiety and Depression Scale (HADS) (0: normal; 21: severe)

Full Information

First Posted
September 24, 2020
Last Updated
August 24, 2021
Sponsor
Epitech Group SpA
Collaborators
Azienda Ospedaliera "Sant'Andrea"
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1. Study Identification

Unique Protocol Identification Number
NCT04568876
Brief Title
Micronized and Ultramicronized Palmitoylethanolamide in COVID-19 Patients
Official Title
Efficacy of Palmitoylethanolamide, in add-on to Standard Therapy, on Inflammatory Markers of Patients With Interstitial Pneumonia Due to COVID-19. A Pilot Controlled, Randomized, Open Lable Clinical Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Completed
Study Start Date
October 23, 2020 (Actual)
Primary Completion Date
February 28, 2021 (Actual)
Study Completion Date
February 28, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Epitech Group SpA
Collaborators
Azienda Ospedaliera "Sant'Andrea"

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
SARS-CoV-2 infection is a condition characterized by excessive leukocyte infiltration, massive release of chemokines, proteases and cytokines, the so-called "cytokine storm", which promote the inflammatory process and contribute to exacerbation of COVID-19 symptomatology. Because of the abnormal release of pro-inflammatory cytokines by non-neuronal cells of the immune system, such as the mast cells in periphery, and microglia at central level, the body activates a defensive neuroinflammatory process that, if not controlled, can become pathological. Therefore it's important to intervene early on neuroinflammation, in order to limit the progression of the disease. A possible intervention is represented by Palmitoylethanolamide (PEA), an endogenous molecule of the N-acylethanolamine family synthesized "on demand" in response to "stress factors" to restore tissue homeostasis, able to control mast cells and microglia uncontrolled activation. Experimental evidence in vitro and in vivo demonstrated the anti-inflammatory and neuroprotective effect of micronized and ultra-micronized PEA (mPEA and umPEA), confirmed in various clinical investigations conducted in patients with different pathological conditions. The aim of this study is to investigate the efficacy of a compound containing mPEA + umPEA on peripheral inflammatory markers, neuroinflammation, and others clinical parameters in intensive care patients with COVID-19 interstitial pneumonia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
PEA Group
Arm Type
Active Comparator
Arm Description
Normast® MPS (mPEA and umPEA 300mg + 600mg) oral suspension: 2700mg/die in 3 doses for 28 days, in add-on to standard therapy
Arm Title
Control Group
Arm Type
Other
Arm Description
Standard therapy only
Intervention Type
Dietary Supplement
Intervention Name(s)
Micronized and ultra-micronized Palmitoylethanolamide (mPEA and umPEA, 300mg + 600mg) oral suspension
Other Intervention Name(s)
Normast® MPS oral suspension
Intervention Description
Micronized and ultra-micronized Palmitoylethanolamide is on the market in Italy as a Food for Special Medical Purposes
Intervention Type
Combination Product
Intervention Name(s)
Standard Therapy
Intervention Description
Standard therapy established for individual patients
Primary Outcome Measure Information:
Title
Number of responder participants after 7 days of treatment
Description
Responder: decrease ≥ 30% from baseline of IL-6 blood levels
Time Frame
7 days
Secondary Outcome Measure Information:
Title
Change of pro-inflammatory markers (IL-6, IL-1 alpha, IL-1 beta, TNF-alpha, PCR, PCT, neopterin)
Time Frame
0, 3, 7, 14, 28 days
Title
Change of anti-inflammatory markers (IL-4, IL-10)
Time Frame
0, 3, 7, 14, 28 days
Title
Change of brain damage markers (S100b, ENS)
Time Frame
0, 3, 7, 14, 28 days
Title
Change of coagulation indices (INR, fibrinogen, D-dimer)
Time Frame
0, 3, 7, 14, 28 days
Title
Change of hematological parameters
Description
leukocyte formula (lymphocytes, CD4 / CD8 ratio)
Time Frame
0, 3, 7, 14, 28 days
Title
Change of oxygenation indices (P/F ratio, lactates)
Time Frame
0, 3, 7, 14, 28 days
Title
Number of participants who developed delirium
Description
Confusion Assessment Method-Intensive Care Unit (CAM-ICU) (0-1: no delirium; >1 delirium)
Time Frame
0, 3, 7, 14, 28 days
Title
Number of participants who developed anxiety and/or depression
Description
Hospital Anxiety and Depression Scale (HADS) (0: normal; 21: severe)
Time Frame
0, 3, 7, 14, 28 days
Other Pre-specified Outcome Measures:
Title
Number of days of invasive mechanical ventilation (orotracheal intubation - IOT)
Time Frame
28 days
Title
Number of days of non-invasive mechanical ventilation (Helmet, face mask)
Time Frame
28 days
Title
Number of days of intensive care (ICU) hospitalization
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Intensive Care Unit Hospitalization for interstitial pneumonia due to COVID-19 diagnosis (nasal swab/sputum/bronchoalveolar lavage positive for Sars-Cov-2 infection) Exclusion Criteria: Pregnancy or breastfeeding; Known allergy or hypersensitivity to the product or its excipients; Inability to take the product per os or via nasogastric tube.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Prof.ssa Flaminia Coluzzi, MD
Organizational Affiliation
Azienda Ospedaliera Universitaria Sant'Andrea di Roma
Official's Role
Principal Investigator
Facility Information:
Facility Name
Anestesia e Rianimazione Azienda Ospedaliera Universitaria Sant'Andrea
City
Roma
ZIP/Postal Code
00189
Country
Italy

12. IPD Sharing Statement

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Micronized and Ultramicronized Palmitoylethanolamide in COVID-19 Patients

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