Standardization of quantity and holding time,for medicated liquids of different physical properties, in the mouth.
- Registration Number
- CTRI/2023/11/059635
- Lead Sponsor
- Mahrashtra University of Health SciencesNashik
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Healthy volunteers willing to participate in the study
2.Equal volunteers of either sex with age matched (Male, Female with same age) between 18 to 60 years including both upper and lower age limit.
1.Volunteers having history of facial paralysis
2.Operated for oral-pharyngeal region.
3.Persons with Chronic nasal obstructive ailments like chronic rhinitis, nasal polyps, Oral Ulcers, Oral thrush (Mukhapaka) or Aphthous ulcers, history of tongue/Cheek Biting, Otitis.
4.Persons with Chronic obstructive ailments of eye such as Glaucoma
5.Pregnant women
6.Volunteers having history of asthma, neural disorders, anti-depressant drug therapy, Bruxism.
7.Volunteers with any sort of habits tobacco, pan, gutaka, alcohol
8.Volunteers having history of consumption of muscle relaxants and antidepressants.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Optimum quantity required to fill oral and vestibular cavity and time taken to start secretions from nose and mouth will be standardizedTimepoint: 60 participants per month will be recruited
- Secondary Outcome Measures
Name Time Method ot applicableTimepoint: Not applicable