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The effectiveness of Mometasone Furoate plus Isotonic Nasal Saline in the Elderly with Rhinitis

The evaluation of the effectiveness of Mometasone Furoate plus Isotonic Nasal Saline in Geriatric Patients with Rhinitis: a Randomized Clinical Trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-498bnq
Enrollment
Unknown
Registered
2018-01-26
Start date
2016-03-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic rhinitis

Interventions

All the 40 individuals included in the study will be submitted to skin prick allergy test, spirometry and blood tests. Furthermore, in these will be measured the peak flow nasal inspiratory before and
Drug

Sponsors

Programa de Pós Graduação em Ciências Médicas da Universidade Federal Fluminense
Lead Sponsor
Hospital Universitário Antônio Pedro
Collaborator

Eligibility

Age
60 Years to 120 Years

Inclusion criteria

Inclusion criteria: Adults with symptoms of chronic rhinitis, two or more symptoms of nasal blockage, rhinorrhea, sneeze or nasal itching for 1 hour or more and for two weeks or more; age equal or above 60 years old; monitored clinically in the departament of allergy and immunology of Hospital Universitário Antônio Pedro.

Exclusion criteria

Exclusion criteria: Primary or secondary immunodeficiency; mechanical obstruction of upper airways; respiratory infection in the last two weeks; impossible to perform spirometry before and after bronchodilator.

Design outcomes

Primary

MeasureTime frame
Improvement in nasal patency of the elderly with rhinitis after two weeks of treatment assessed by the peak nasal inspiratory flow (PNIF). That is, increase of at least 30 L/min in the PNIF after two weeks of treatment.

Secondary

MeasureTime frame
Reduction of at least 15 points in the sinonasal outcome test (SNOT-22) of the elderly with rhinitis after two weeks of treatment;Reduction of at least 2 points in the severity of symptoms assessed by a 10-point visual analogic scale (VAS) of the elderly with rhinitis after two weeks of treatment

Countries

Brazil

Contacts

Public ContactJosé Laerte;Victor Morandi;de Carvalho

Hospital Universitário Antônio Pedro;Hospital Universitário Antônio Pedro

jlboechat.alergo@gmail.com;torcortes@yahoo.com.br552126299254;552126299254

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Mar 1, 2026