NCT00877461

Completed

Glucose Monitor Accuracy Investigation (Ⅰ)

National Taiwan University Hospital Source

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Other study identifiers

Sponsor study identifier

9461700317

Study Type

observational

Actual enrollment (reported)

308

Locations

1 country

Sites

1

Timeline

Study Start

May 2005

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

November 2005

Actual (reported)

Study Completion

December 2005

Actual (reported)

Brief Summary

According to Section 7.3 and Section 7.4, ISO 15197(2003), it adopts the whole blood of fingertips and vein as samples to evaluate the accuracy of portable BGM.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 308 participants
Study completion date: December 2005
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
May 2005
Date type not reported
This date has not been verified as actual or estimated.
Primary Completion
November 2005
Actual (reported)
Study Completion
December 2005
Actual (reported)
First Submitted
April 6, 2009
Actual (reported)
First Posted
April 7, 2009
Actual (reported)

Last Updated: April 8, 2009
Status Verified: April 2009
Last Update Submitted: April 7, 2009

Conditions

Healthy

Outcome Measures

Primary Outcomes (1)

glucose
10 min

Eligibility Criteria

Age15 Years - 70 Years

Sexall

Healthy VolunteersYes

Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

The glucose concentrations of volunteer shall be distributed as specified in ISO15197 Table 3

You may qualify if:

volunteers with diabetes and non-diabetes

You may not qualify if:

Sponsors & Collaborators

National Taiwan University Hospital
Otherlead

Study Sites (1)

National Taiwan University Hospital

Taipei, Taiwan

Study Officials

Feng-Huei Lin, PhD
Biomedical Engineering Department of National Taiwan University Hospital
STUDY DIRECTOR

Enrollment

308 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: CASE ONLY
Time Perspective: CROSS SECTIONAL
Sponsor Type: OTHER

Study Record Dates

First Submitted

April 6, 2009

First Posted

April 7, 2009

Study Start

May 2005

Date type not reported

This date has not been verified as actual or estimated.

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Contact the study team to confirm eligibility.

Primary Completion

November 2005

Actual (reported)

Study Completion

December 2005

Actual (reported)

Last Updated

April 8, 2009

Record last verified: 2009-04

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT00877461
Data provider: ClinicalTrials.gov
Source updated: 2009-04-08
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:33:52 UTC

Locations

TW(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

Primary Completion

Study Completion

First Submitted

First Posted

Conditions

Outcome Measures

Primary Outcomes (1)

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Enrollment

Study Design

Study Record Dates

Source record

Locations