Evaluation of the Effects of Treatment With Bioarginin C in Adult Subjects Belonging to the Post-Covid Day Hospital

NCT ID: NCT04947488

Last Updated: 2022-05-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-06-18

Study Completion Date

2022-11-18

Brief Summary

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Long Covid could be much more frequent than it is thought to be. Few dwell on the great problem represented by the post covid syndrome. The virus often leaves important marks on our body, and those who recover face problems of various kinds: chronic fatigue, shortness of breath, dry cough, headache, cognitive difficulties.

On the duration and resolution of this syndrome, now recognized as a highly debilitating condition, there are still no great answers: for this reason it is always important to emphasize that contracting Covid, even in a not serious form, still means exposing oneself to long-term risks that are still not well codified by the scientific community. Guidelines and more tools are expected to best assist these patients.

Detailed Description

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Conditions

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Fatigue Syndrome, Chronic Inflammation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Bioarginina C

vials based on L-arginine and liposomal vitamin C

Group Type ACTIVE_COMPARATOR

Bioarginina C

Intervention Type DIETARY_SUPPLEMENT

Dietary supplement vials

Placebo

vials without L-arginine and liposomal vitamin C

Group Type PLACEBO_COMPARATOR

Bioarginina C

Intervention Type DIETARY_SUPPLEMENT

Dietary supplement vials

Interventions

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Bioarginina C

Dietary supplement vials

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

subjects with proven positivity to the molecular test for Sars-cov2 with demonstration of microbiological healing patients discharged from FPG or other hospital structures; or only contact in PS; or home management age: range 20-60 years Fatigue operationalized as an affirmative answer to item "7" (CES-D)

Exclusion Criteria

Pharmacological therapies with possible interactions with the mechanisms / processes under study (e.g. antihypertensive drugs, cortisone drugs, NSAIDs, immunosuppressants, nitrates)
Minimum Eligible Age

20 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Milan

OTHER

Sponsor Role lead

Responsible Party

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Matteo Tosato

Doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Barbara Maglione

Napoli, , Italy

Site Status RECRUITING

Countries

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Italy

Central Contacts

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barbara maglione

Role: CONTACT

+393343293357 ext. +393343293357

Facility Contacts

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barbara o maglione

Role: primary

+393343293357 ext. +393343293357

Other Identifiers

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Bioarginina C

Identifier Type: -

Identifier Source: org_study_id

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