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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05508425
Other study ID # IRB2021110
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 1, 2021
Est. completion date July 5, 2022

Study information

Verified date August 2022
Source Chiayi Christian Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To assess the effect of water temperature and additives on pregnant women's taste and side effect during the oral glucose tolerance test (OGTT) evaluation.


Recruitment information / eligibility

Status Completed
Enrollment 400
Est. completion date July 5, 2022
Est. primary completion date July 5, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria: - Pregnant women - Gestational age between 24 and 28 weeks Exclusion Criteria: - Clinical diagnosis of overt type 2 diabetes - Clinical diagnosis of facial palsy - Clinical diagnosis of oral cavity and throat - Clinical diagnosis of hypothyroidism - Clinical diagnosis of chronic hepatitis - Clinical diagnosis of kidney disease .Clinical diagnosis of Sicca syndrome.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
oral glucose tolerance test using water at room temperature
The use of water at room temperature to solve the 75g glucose.
oral glucose tolerance test using hot water
The use of hot water to solve the 75g glucose.
oral glucose tolerance test using cold water
The use of cold water to solve the 75g glucose.
oral glucose tolerance test using hot water with tea bag
The use of hot water with tea bag to solve the 75g glucose.
oral glucose tolerance test using room temperature water with tea bag
The use of room temperature water with tea bag to solve the 75g glucose.
oral glucose tolerance test using cold water with tea bag
The use of cold water with tea bag to solve the 75g glucose.
Oral glucose tolerance test using bubble water at room temperature
The use of bubble water at room temperature to solve the 75g glucose.
Oral glucose tolerance test using bubble water
The use of cold bubble water to solve the 75g glucose.

Locations

Country Name City State
Taiwan Ditmanson Medical Foundation Chia-Yi Christian Hospital Chiayi City

Sponsors (1)

Lead Sponsor Collaborator
Chiayi Christian Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Glycaemia level Glycaemia level just before glucose administration Glycaemia level was measured just before glucose administration.
Primary Glycaemia level Glycaemia level at 1 hour after glucose administration Glycaemia level was measured at 1 hour after glucose administration
Primary Glycaemia level Glycaemia level at 2 hour after glucose administration Glycaemia level was measured at 2 hours after glucose administration
Primary gestational diabetes mellitus gestational diabetes mellitus just before glucose administration. Just before glucose administration.
Primary gestational diabetes mellitus gestational diabetes mellitus at 1 hour after glucose administration. At 1 hour after glucose administration
Primary gestational diabetes mellitus gestational diabetes mellitus at 2 hour after glucose administration. At 2 hour after glucose administration
Primary Satisfaction after glucose solution administration Satisfaction was measured by a questionnaire using 5-point Likert scale (1: very dissatisfied; 2: dissatisfied; 3: neutral; 4: satisfied; 5: very satisfied). Just after glucose administration
Primary Taste after glucose solution administration Taste was measured by a questionnaire using 5-point Likert scale (1: very dissatisfied; 2: dissatisfied; 3: neutral; 4: satisfied; 5: very satisfied). Just after glucose administration
Primary Nausea after glucose solution administration Nausea was measured by a questionnaire using 5-point Likert scale (1: not at all; 2: slightly; 3: neutral; 4: serious; 5: very serious) Just after glucose administration
Primary Vomiting after glucose solution administration Vomiting was measured by a questionnaire using 5-point Likert scale (1: not at all; 2: slightly; 3: neutral; 4: serious; 5: very serious) Just after glucose solution administration
Primary Headache after glucose solution administration Headache was measured by a questionnaire using 5-point Likert scale (1: not at all; 2: slightly; 3: neutral; 4: serious; 5: very serious) Just after glucose solution administration
Primary Abdominal bloating after glucose solution administration Abdominal bloating was measured by a questionnaire using 5-point Likert scale (1: not at all; 2: slightly; 3: neutral; 4: serious; 5: very serious) Just after glucose solution administration
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