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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04900753
Other study ID # 201901244A3
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 25, 2019
Est. completion date September 30, 2020

Study information

Verified date October 2019
Source Chang Gung Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To investigate the risk factors related to xerostomia (dry mouth) after surgery


Description:

Dry mouth of postoperative makes the patient feel thirst, and the pain of the lips is cracked. It will also make the sputum thick and sticky, making it difficult for the patient to cough by himself. Especially the elderly may have sputum accumulation and pneumonia. The incidence of dry mouth was 88%, 6-8 hours after abdominal surgery. Initiating the motivation of this study, it is hoped that through research to understand the relevant factors causing dry mouth after surgery.


Recruitment information / eligibility

Status Completed
Enrollment 472
Est. completion date September 30, 2020
Est. primary completion date March 31, 2020
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: 1. Hospitalized patients 2. Elective surgery patients 3. >19 years old patients Exclusion Criteria: 1. cognitive impairment patients 2. ICU patients

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan Hsiu-Ling Yang Taoyuan No.5, Fuxing St., Guishan Dist

Sponsors (1)

Lead Sponsor Collaborator
Chang Gung Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary To investigate the risk factors related to xerostomia (dry mouth) after surgery To investigate the risk factors related to xerostomia (dry mouth) after surgery 5 mins
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