- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05241587
Chewing Gum in Hemodialysis Patients
Evaluation of the Effect of Xylitol Gum on Thirst, Dry Mouth and Nausea in Patients Undergoing Haemodialysis
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Trabzon, Turkey, (554) 326-3222
- Karadeniz Techinical University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 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 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). |
|
Experimental: 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: 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. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effect of chewing xylitol gum on thirst
Time Frame: 6 weeks
|
Thirst were evaluated with "Visual Analog Score".
VAS is a 10 cm or 100 mm long measuring instrument on a horizontal line with two different ends.
The left end of the line is marked as "no" and the right end as "worst".
|
6 weeks
|
|
Effect of chewing xylitol gum on dry mouth
Time Frame: 6 weeks
|
Dry Mouth were evaluated with "Visual Analog Score".
VAS is a 10 cm or 100 mm long measuring instrument on a horizontal line with two different ends.
The left end of the line is marked as "no" and the right end as "worst".
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effect of Xylitol Gum on nausea.
Time Frame: 6 weeks
|
Xylitol Gum on nausea in patients undergoing haemodialysis.
Nausea was evaluated with Rhodes Nausea, Vomiting and Retching Index.
The highest possible value in the index is 32, which indicates the most severe symptom for the patient.
|
6 weeks
|
|
Effect of Xylitol Gum on salivary flow rate.
Time Frame: 6 weeks
|
Xylitol Gum on salivary flow rate in patients undergoing haemodialysis.
Salivary flow rate with Saliva Flow Rate Measurement Tool (Graded Tube).Saliva flow >0.25 mL/min was considered "normal"; 0.1-0.25 mL/min "low"; <0.1 mL/min "hyposalivation"
|
6 weeks
|
|
Effect of Xylitol Gum on oral pH.
Time Frame: 6 weeks
|
Xylitol Gum on oral pH in patients undergoing haemodialysis.
Salivary pH with Oral Environment pH Measurement Tool (pH Meter).
When the pH meter electrode is immersed in saliva, the pH value of the saliva is determined by the pH value on the screen.
"0-6 pH" appearing on the pH meter screen is considered acidic, "7 pH" neutral, and "8-14 pH" alkaline"
|
6 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Didem Sarımehmet, PhD, Karadeniz Techinical University
- Principal Investigator: Sevilay Hintistan, PhD, Karadeniz Techinical University
Publications and helpful links
General Publications
- 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.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Nurse_haemo01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Nausea
-
Hafiz Muhammad HamzaFederal Government Polyclinic (Postgraduate Medical Institute)CompletedPostoperative Nausea and Vomiting (PONV)Pakistan
-
University of North Carolina, Chapel HillNational Institute of Dental and Craniofacial Research (NIDCR)CompletedPost-operative Nausea | Post-operative Vomiting | Nausea PersistentUnited States
-
Cukurova UniversityTarsus UniversityCompletedNausea, Postoperative | Vomiting, Postoperative | APFEL RİSK SCORETurkey
-
MonoSol RxCompletedNausea With Vomiting Chemotherapy-Induced | Nausea and Vomiting, PostoperativeIndia
-
GlaxoSmithKlineCompletedPostoperative Nausea and Vomiting | Nausea and Vomiting, PostoperativeUnited States, Spain, Philippines, Israel, Hong Kong, Thailand, United Kingdom, Hungary, Slovenia, Norway, Denmark
-
Lancaster General HospitalCompletedBariatric Surgery Candidate | Nausea, PostoperativeUnited States
-
Benaroya Research InstituteVirginia Mason Hospital/Medical CenterRecruitingPost Operative Nausea and VomitingUnited States
-
Hoffmann-La RocheCompletedPost-Operative Nausea and VomitingUnited States
-
Cairo UniversityUnknownPost Operative Nausea and VomitingEgypt
-
Yonsei UniversityCompletedPost Operative Nausea and VomitingKorea, Republic of
Clinical Trials on Gum Group:
-
TC Erciyes UniversityCompletedAcute Pancreatitis | ThirstTurkey
-
Çankırı Karatekin UniversityCompleted
-
University of British ColumbiaCompleted
-
Hacettepe UniversityCompletedQuality of Life | Breast Cancer | Nausea and Vomiting | Chewing GumTurkey (Türkiye)
-
Marmara UniversityCompleted
-
Chiayi Christian HospitalNot yet recruiting
-
Hospital de Clinicas de Porto AlegreCompletedMetabolic Syndrome | AlbuminuriaBrazil
-
University of NottinghamTasteTechCompletedAnosmia | Dysgeusia | Ageusia | Parosmia | PhantosmiaUnited Kingdom
-
Ege UniversityCompleted