NCT04900753

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
472

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2019

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 25, 2019

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2020

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2020

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

May 20, 2021

Completed
5 days until next milestone

First Posted

Study publicly available on registry

May 25, 2021

Completed
Last Updated

February 10, 2023

Status Verified

October 1, 2019

Enrollment Period

5 months

First QC Date

May 20, 2021

Last Update Submit

February 8, 2023

Conditions

Postoperative Complications

Outcome Measures

Primary Outcomes (1)

  • 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

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

over 19 years old elective surgery patients

You may qualify if:

  • Hospitalized patients
  • Elective surgery patients
  • \>19 years old patients

You may not qualify if:

  • cognitive impairment patients
  • ICU patients

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hsiu-Ling Yang

Taoyuan District, No.5, Fuxing St., Guishan Dist, 333, Taiwan

Location

MeSH Terms

Conditions

Postoperative Complications

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 20, 2021

First Posted

May 25, 2021

Study Start

October 25, 2019

Primary Completion

March 31, 2020

Study Completion

September 30, 2020

Last Updated

February 10, 2023

Record last verified: 2019-10

Data Sharing

IPD Sharing
Will not share

Locations

TW(1)