NCT04977739

Brief Summary

Fluorescence is one of the most commonly used research and detection techniques in the field of biomedical science. The characteristics of fluorescent probe directly affect the performance and application of fluorescence analysis and imaging. Aggregation-Caused Quenching has limited the application of traditional fluorescent probes to some extent. This project intends to systematically evaluate the detection efficiency of new methods through the detection of biomarkers in clinical samples and the comparison with the detection methods of traditional biomarkers, so as to provide theoretical and experimental basis for the establishment of fast and simple biomarker detection technologies with new biological probes.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
737

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2021

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

First Submitted

Initial submission to the registry

July 14, 2021

Completed
13 days until next milestone

First Posted

Study publicly available on registry

July 27, 2021

Completed
7 days until next milestone

Study Start

First participant enrolled

August 3, 2021

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 15, 2022

Completed
10 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 25, 2022

Completed
Last Updated

August 22, 2022

Status Verified

June 1, 2021

Enrollment Period

12 months

First QC Date

July 14, 2021

Last Update Submit

August 19, 2022

Conditions

Outcome Measures

Primary Outcomes (1)

  • signal intensity of the probes

    one day

Study Arms (2)

those with a condition

Diagnostic Test: No intervention

those without a condition

Diagnostic Test: No intervention

Interventions

No interventionDIAGNOSTIC_TEST

No intervention

those with a conditionthose without a condition

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

NanFang Hospital samples

You may qualify if:

  • Sign the informed consent form voluntarily.
  • Age 18-70 years old.
  • High expression (positive) group: The results of multiple laboratory tests indicate that the marker is higher than the normal range.
  • Low expression (negative) healthy volunteer group: those with no underlying diseases and no abnormalities in the physical examination.
  • Have routine examination to check the remaining body fluid samples, and the body fluid samples are not contaminated.

You may not qualify if:

  • Accompanied by other inflammations.
  • The data of the subject is not complete, or the collection of cases is incomplete due to other reasons.
  • The researcher judged that it was not suitable to participate in this research.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nanfang Hospital

Guangzhou, Guangdong, 510515, China

Location

MeSH Terms

Conditions

NeoplasmsCardiovascular DiseasesRespiratory Tract DiseasesDigestive System DiseasesEndocrine System DiseasesMetabolic DiseasesImmune System DiseasesUrologic DiseasesNervous System DiseasesHematologic DiseasesCommunicable Diseases

Condition Hierarchy (Ancestors)

Nutritional and Metabolic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesHemic and Lymphatic DiseasesInfectionsDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Bo Situ

    Nanfang Hospital, Southern Medical University

    STUDY DIRECTOR

Study Design

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

Study Record Dates

First Submitted

July 14, 2021

First Posted

July 27, 2021

Study Start

August 3, 2021

Primary Completion

July 15, 2022

Study Completion

July 25, 2022

Last Updated

August 22, 2022

Record last verified: 2021-06

Locations