Chewing Gum in Hemodialysis Patients
Mouth Dryness, Nausea, Hemodialysis Complication
About this trial
This is an interventional health services research trial for Mouth Dryness
Eligibility Criteria
Inclusion Criteria:
- being 18 years or older,
- being able to speak and understand Turkish,
- being oriented to person, place and time,
- receiving haemodialysis treatment for at least three months,
- experiencing dry mouth, thirst and nausea,
- not having any chewing difficulties,
- not having any dental prosthesis for the gum group,
- using mouth spray for the last two weeks at the request of the physician for the mouth spray group.
Exclusion Criteria:
- exclusion criteria included having a mental,
- hearing and speech impediment,
- being diagnosed with a psychiatric disease,
- using antiemetic drugs, being diagnosed with Sjögren's syndrome,
- receiving radiotherapy or chemotherapy,
- having a salivary gland infection,
- previous salivary gland surgery,
- sucking on ice cubes, chewing mint/lemon peels, and using mouthwash.
Sites / Locations
- Karadeniz Techinical University
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
The chewing gum group
The mouth spray group
Gum group patients consisted of patients who chewed "Xylitol Granule Filled Dragee Sugar Free Gum/Xylitol Gum/First X-Fresh". It is reported that the use of xylitol five times a day (not less than three times) is appropriate and effective (Xylitol, 2020; Xylitol, 2006; Llop, et al., 2010). Therefore, this group of patients was allowed to chew xylitol gum for 10 minutes, five times a day for six weeks.
The patients in the mouth spray group included those who had been using Oral Spray/Act Dry Mouth Spray regularly as two puffs three times a day at the request of the physician for the last two weeks. This group of patients continued to use the mouth spray at the physician's request.