Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
75 participants
INTERVENTIONAL
2018-03-03
2020-12-12
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
SINGLE
Study Groups
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The chewing gum 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.
Gum Group:
Gum 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).
The mouth spray group
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.
Mouth Spray Group:
Mouth Spray Group:
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.
Interventions
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Gum Group:
Gum 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).
Mouth Spray Group:
Mouth Spray Group:
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.
Eligibility Criteria
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Inclusion Criteria
* 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
* 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.
18 Years
ALL
Yes
Sponsors
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Didem Sarımehmet
OTHER
Responsible Party
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Didem Sarımehmet
Lecturer
Principal Investigators
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Didem Sarımehmet, PhD
Role: PRINCIPAL_INVESTIGATOR
Karadeniz Techinical University
Sevilay Hintistan, PhD
Role: PRINCIPAL_INVESTIGATOR
Karadeniz Techinical University
Locations
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Karadeniz Techinical University
Trabzon, , Turkey (Türkiye)
Countries
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References
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Almutary H, Bonner A, Douglas C. Symptom burden in chronic kidney disease: a review of recent literature. J Ren Care. 2013 Sep;39(3):140-50. doi: 10.1111/j.1755-6686.2013.12022.x. Epub 2013 Jul 4.
Akgöz N, Arslan S (2017). Examination of Symptoms in Patients Who are on Hemodialysis Treatment. Journal of Nephrology Nursing, 12(1): 20-28.
Other Identifiers
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Nurse_haemo01
Identifier Type: -
Identifier Source: org_study_id
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