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Evaluation of the Efficacy of Topical Steroid Spray Therapy in Recurrent Chronic Rhinosinusitis

Evaluation of the Efficacy of Topical Steroid Spray Therapy in Recurrent Chronic Rhinosinusitis - Efficacy of Topical Steroid Spray in Recurrent Chronic Rhinosinusitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055047
Enrollment
84
Registered
2024-07-24
Start date
2024-08-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Chronic rhinosinusitis with nasal polyps

Interventions

In drug spraying using a flexible endoscope through a treatment channel group, the doctor inserts the flexible endoscope with a treatment channel into the sinus cavity to be treated, confirms the trea
s treatment channel, and sprays the drug with a syringe attached to the spraying catheter. In drug spraying using a rigid endoscope through an otorhinolaryngologic catheter group, the doctor inserts t

Sponsors

Dokkyo Medical University
Lead Sponsor
KEIHOKAI, Medical Corporation, MATSUWAKI CLINIC Shinagawa OLYMPUS MEDICAL SYSTEMS CORPORATION
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients over 18 years of age. Patients diagnosed with chronic rhinosinusitis with nasal polyp. Patients with a history of endoscopic sinus surgery and postoperative recurrence despite saline lavage of the sinuses and continuous nasal steroid spray treatment. Patients who have received a thorough explanation of their participation in this study and have given written consent of their own free will based on a thorough understanding.

Exclusion criteria

Exclusion criteria: Patients with allergy or intolerance to steroids. Patients with comorbid conditions require chemotherapy, immunotherapy, or oral steroids. Patients with clinical evidence of acute bacterial sinusitis, invasive fungal sinusitis, or diabetes mellitus. Patients with a history or diagnosis of glaucoma, ocular hypertension, or cataracts. Other patients were deemed inappropriate by the physician.

Design outcomes

Primary

MeasureTime frame
Changes in edematous lesions of the sinonasal mucosa according to endoscopic findings before the treatment and one month after the treatment in the spraying of steroids through an otolaryngological catheter under the observation of a rigid endoscope or through a scope channel using a flexible endoscope.

Secondary

MeasureTime frame
Changes in CT findings before and one month after treatment Availability of steroid sprays and difficulty of accessing the spray catheter to the treatment area Changes in scores and percentages on the symptom questionnaire and the patient tolerance questionnaire

Countries

Japan

Contacts

Public ContactTsuguhisa Nakayama

Dokkyo Medical University Hospital Otorhinolaryngology and Head & Neck Surgery

t-nakayama855@dokkyomed.ac.jp0287-87-2164

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026