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Steam Inhalations in COVID-19 Patients (Steam-COVID)

M

Meyer Children's Hospital IRCCS

Status

Terminated

Conditions

Covid19
Coronavirus
Coronavirus Infection

Treatments

Procedure: Steam inhalations

Study type

Interventional

Funder types

Other

Identifiers

NCT04743349
Steam-COVID

Details and patient eligibility

About

The new coronavirus (SARS-CoV-2) causing COVID-19 is an RNA virus coated with a capsid and a peri-capsid crossed by glycoprotein structures. The external proteic structure, which attacks human cells, is a potential target to therapeutic interventions against virus replication in airways.

Since high temperature can cause irreversible denaturation of proteins and loss of SARS CoV and SARS CoV-2 infectivity was obtained after heating at 56 ◦C for 15 and 30 min in liquid environments respectively, we designed a protocol aimed at damaging SARS-CoV-2 capsid through steam inhalation cycles. Although the ominous consequences of COVID 19 infections has directed medical attention toward solidly established medical approaches, the European Pharmacopoeia VI edition also quotes steam inhalations as a procedure to treat of respiratory diseases.

Based on these suggestions we established a quasi-randomized clinical trial enrolling 200 asymptomatic or paucisymptomatic patients in whom rhino-pharyngeal-swab revealed a SARS-CoV-2 infection. The study protocol consisted of exposure of airway mucosae to humidified steam (pH 8 per NaHCO3 and hypertonic 15 g/L NaCl) through steam inhalation for at least 20 min (4 cycles of 5 min) daily, for 10 days.

The objective of the study is to reduce the viral shedding using steam inhalations.

Enrollment

143 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults with a SARS-CoV-2 positive molecular swab carried out in the previous 48 hours before the enrollement
  • Adults with mild infection
  • Adults with symptoms such as fever above 37 ° C, feeling bad, cold symptoms (cough, pharyngodynia, nasal congestion), headache, myalgia, diarrhea, anosmia, dysgeusia
  • Adults without the above symptoms

Exclusion criteria

  • Adults with dyspnea and/or dehydration and/or alterations in consciousness and/or sepsis.
  • Subjects with severe asthma
  • Subjects and with contraindications to treatment with steam inhalations
  • Multi-allergic subjects
  • Subjects unable to complete the protocol

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

143 participants in 2 patient groups

Experimental arm
Experimental group
Description:
Steam inhalations
Treatment:
Procedure: Steam inhalations
Control arm
No Intervention group
Description:
No intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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