Dry Mouth Clinical Trial
Official title:
Experimental Study to Evaluate the Effectiveness of an Intervention Bundle on Thirst Intensity and Dry Mouth Among Patients of Selected Units
The study evaluates the effectiveness of an Intervention Bundle on Thirst Intensity and Dry Mouth among Patients admitted in ICUs. Patients were randomized into two groups - Experimental and Control group. Experimental group received intervention Bundle whereas control group didn't receive any intervention. Usual care was continued in both the groups.
The Convenience sampling technique was used to select Maharishi Markandeshwar institution of
Medical Science and Researches Hospital, Mullana, Ambala. Intensive Care Units and a total of
60 patients in those units were also selected conveniently. The selected patients were
randomly assigned to experimental and control group using lottery method. The total sample
size for the study was 60 patients i.e. - 30 in experimental group and 30 in control group.
Experimental Group -patients were explained regarding administration of intervention
bundle.Assessment of patients' mouth and lips was determined firstly. Intervention bundle
consisted of sterile cold wet oral swab wipes and sterile ice cold water sprays administered
for in two sessions of 15 minutes each. First session was given in 15 minutes, patients
received cold wet oral swab wipes in oral cavity 2 to 3 times and mouth spray with 5 to 6
sprays. A maximum of 9 wipes and 18 sprays of sterile water. After administration of
intervention bundle, Post test 1 was taken after 15 minutes observation with the same tools.
Then researcher waited for 15 minutes after post test1 and session two was administered in 15
minutes with a maximum of 9 wipes and 18 sprays of sterile water. Post test 2 was taken after
15 minutes of session two.
Control group: control group was not given any intervention. Sample characteristics and
clinical data (variables) were recorded in record sheet and thirst intensity and dry mouth
scores were assessed only. After 30 minutes of pre test scores, post test 1 was taken and
data were recorded. Then after, 30 minutes of post test 1, post test 2 was taken and data
were recorded.
(Intervention to the control group was given after accomplishment of Post test for ethical
consideration).
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT04914208 -
Effect of Wearing Face Masks on Salivary Parameters and Halitosis
|
N/A | |
| Completed |
NCT00601211 -
Bioequivalency Study of 5 mg Piolocarpine Tablets Under Fed Conditions
|
N/A | |
| Completed |
NCT00601874 -
Bioequivalency Study of 5 mg Pilocarpine Tablets Under Fasting Conditions
|
N/A | |
| Completed |
NCT04152642 -
A Pilot Study to Assess Dry Mouth Relief After Using an Experimental Mouth Rinse
|
N/A | |
| Completed |
NCT04632004 -
Questionnaire Regarding the Effect of Wearing Face Masks on Oral Health
|
N/A | |
| Completed |
NCT05640362 -
Efficacy of Natural Enzymes Mouthwash: a Randomised Controlled Trial
|
N/A | |
| Completed |
NCT04986501 -
Clinical Evaluation of MucoPEG™ for Xerostomia
|
N/A | |
| Completed |
NCT04189081 -
Improvement of Dry Mouth Sufferers After Using an Experimental Dry Mouth Rinse Compared to a Water Control
|
N/A | |
| Completed |
NCT05871580 -
Effect to the Photobiomodulation in the Burning Mouth Syndrome
|
N/A | |
| Completed |
NCT06258603 -
Oral Care of Intubated Intensive Care Patient
|
N/A | |
| Completed |
NCT01647737 -
Green Tea Lozenges for the Management of Dry Mouth
|
Phase 1/Phase 2 | |
| Completed |
NCT01737307 -
Effect of Fluoride Varnish and CPP-ACP on Oral and Salivary Symptoms During Chemotherapy
|
Phase 2 | |
| Active, not recruiting |
NCT03874572 -
Allogeneic Mesenchymal Stem Cells for Radiation-induced Hyposalivation and Xerostomia/Dry Mouth
|
Phase 1 | |
| Completed |
NCT03035825 -
Efficacy of Oral Moisturizing Jelly on Oral Health and Nutrition in Post-radiotherapy Head and Neck Cancer Patients
|
N/A | |
| Recruiting |
NCT05964959 -
A Mouth Education Program for Dry Mouth
|
N/A | |
| Withdrawn |
NCT02123147 -
Examining the Immunological Process of Autoimmune Patients
|
N/A | |
| Completed |
NCT01885065 -
Efficacy of Novel Edible Gel-based Artificial Saliva in Cancer Patients
|
N/A | |
| Completed |
NCT03281486 -
"Hyaluronan" Formulation for Type 2 Diabetic Patients With Dry Mouth
|
N/A | |
| Not yet recruiting |
NCT05506137 -
Xerostomia in Patients With a Life-limiting Condition or Frailty
|
Phase 3 | |
| Completed |
NCT01690052 -
Efficacy of Cevimeline Versus Pilocarpine in the Secretion of Saliva
|
N/A |