Cleanoze® Irrigation Device With Powder Preparation Versus Conventional Irrigation Method for Chronic Rhinitis
- Conditions
- Rhinitis
- Interventions
- Drug: Cleanoze®Drug: Saline (Syringe irrigation)
- Registration Number
- NCT02763241
- Lead Sponsor
- Khon Kaen University
- Brief Summary
The investigators proposed that the Cleanoze® is superior to the traditional nasal saline irrigation in term of the ease of use which will resulting in a better quality of life of the participants. This study will compared the efficacy, adverse reactions, complications and ease of use of Cleanoze® comparing with normal saline solution
- Detailed Description
Cleanoze® consists of a powder made up of Sodium chloride and Sodium Bicarbonate. This powder when dissolved in 250 ml of water is closely resembles the content of a body fluid which normally baths the outside of the cells of the body. This fluid is isotonic solution.
The nasal saline irrigation is the common procedure for upper respiratory tract infection patients including chronic rhinitis. The physician usually order the normal saline with appropriate medication e.g. anti-histamines, nasal steroids and anti-biotics to treat this condition.
The investigators proposed that the Cleanoze® is superior to the traditional nasal saline irrigation in term of the ease of use which will resulting in a better quality of life of the participants. This study will compared the efficacy, adverse reactions, complications and ease of use of Cleanoze® comparing with normal saline solution.
Study Population: Any patients with chronic rhinitis (e.g. allergic rhinitis, vasomotor rhinitis) will be randomized to receive the study or control medication. The investigators will include the children 5 years and above which able to doing the lavage under the parents assistant or by them self.
Study Design: Phase III randomized controlled trial
Sample Size: Estimate from pilot study, the 71 patients per arm was estimated (142 participants totally).
Study Duration:
* Duration of enrollment is 1 year.
* The patients will be followed up to 1 months depend on the disease conditions.
* The data analysis will take 3 additional months
* The full report will complete after the data analysis within 3 months
* The total of 1 year and 6 months period needed for this study.
Primary Objective: To compare the satisfaction of the patients using Cleanoze® versus conventional device
Secondary Objective(s):
* The adherence to Cleanoze® device
* The durability of the Cleanoze® device
* The patient symptom score (VAS)
* The SNOT-22 questionaire for evaluating the quality of life of the patients
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 115
- Any patients with chronic rhinitis conditions regardless of any cause (e.g. allergic, irritant, infection)
- Acute or chronic rhinosinusitis
- Acute nasopharyngitis (common cold)
- Patients with a tendency to aspirate such as cerebrovascular accident, cranio-facial diseases.
- Sinunasal, nasopharyngeal and skull base tumors
- Age under 5 years old.
- Cannot administer a saline irrigation under the assistant of a care giver.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Cleanoze® Cleanoze® Cleanoze® consists of a powder made up of Sodium chloride and Sodium Bicarbonate. This powder when dissolved in 250 ml of water is closely resembles the content of a body fluid which normally baths the outside of the cells of the body. This fluid is isotonic solution. The patient will be instructed to use this isotonic solution for nasal irrigation daily. Syringe irrigation Saline (Syringe irrigation) Nasal irrigation using sterile 0.9% NaCl 250 ml by 20 ml syringe The patient will be instructed to use this isotonic solution for nasal irrigation daily.
- Primary Outcome Measures
Name Time Method Satisfaction score 1 month This score will be evaluated at the end of 1 month using using the satisfaction questionaire
- Secondary Outcome Measures
Name Time Method The symptoms score of the patients 1 month The symptoms score will be evaluated using the one-question VAS scale
The durability of the Cleanoze® device 1 month The durability will be evaluated by inspecting the device at the end of 1 month period
The Sino-Nasal Outcome Test-22 Questionnaire (SNOT-22) score 1 month The SNOT-22 score will be evaluated by using SNOT-22 questionnaire
The adherence to Cleanoze® devic 1 month The adherence will be evaluated by the diary that the investigator given to the participants
Adverse events 1 month The adverse events will be recorded in the case record form at follow-up time
Trial Locations
- Locations (1)
Department of Otolaryngology, Khonkaen University
🇹🇭Muang, Khonkaen, Thailand