Urine VOC Investigation in Bladder Cancer Diagnosis

Sponsor
First Affiliated Hospital Xi'an Jiaotong University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05671289
Collaborator
(none)
65
1
10.7
6.1

Study Details

Study Description

Brief Summary

The goal of this study to investigate the volatile organic compounds (VOCs) in the urine samples of both healthy individual and bladder cancer patients, using gas chromatography - mass spectrometry. Researchers aim to find a set of certain VOCs specific to bladder cancer and use this set to construct a diagnostic model that can help diagnosing bladder cancer. Participants will be asked to collect their early morning midstream urine in a predesignated container. Researchers will compare urine VOCs from bladder cancer patients and healthy individuals to see if there is any VOC whose concentration differ significantly among the two groups.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: analysis of urine volatile organic compounds

Detailed Description

Specifically, participants will be asked to collect 35-45 ml of their early morning midstream urine sample in a predesignated polytetrafluoroethylene bottle. Researcher will collect participants' health information, including their: 1)smoking history; 2)comorbidity; 3) history of past urological procedure; 4)medication; 5)pathology diagnosis after surgery, if participants have bladder cancer.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
65 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Investigation of Urine Volatile Organic Compounds as Novel Diagnostic Biomarker in Bladder Cancer
Actual Study Start Date :
Nov 10, 2022
Anticipated Primary Completion Date :
May 1, 2023
Anticipated Study Completion Date :
Oct 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Patients with confirmed bladder tumor

Patients with bladder tumor, confirmed by cystoscopy and radiology. Age ranging from 18 to 80 years old. Women of childbearing age should have negative urine pregnancy test.

Diagnostic Test: analysis of urine volatile organic compounds
gas chromatography - mass spectrometry will be used to assess the composition of VOCs in urine samples of all participants.

Healthy volunteers

Individuals with no known disease and normal urinalysis. Age ranging from 18 to 80 years old. Women of childbearing age should have negative urine pregnancy test.

Diagnostic Test: analysis of urine volatile organic compounds
gas chromatography - mass spectrometry will be used to assess the composition of VOCs in urine samples of all participants.

Outcome Measures

Primary Outcome Measures

  1. Urine volatile organic compounds composition of all urine samples [immediately after GC-MS analysis has been finished]

    Data derived from mass spectrums of GC-MS measurement of VOC components in urine samples, including VOC components identified comparing obtained data to those in public GC-MS database and the absolute concentration of VOCs identified.

Secondary Outcome Measures

  1. Pathological diagnosis of bladder tumor patients enrolled [Immediately after the release of pathological examination reports by pathology department in the First affiliated hospital of Xi'an jiaotong university]

    Staging of bladder cancer using American Joint Committee on Cancer (AJCC) TNM system and histology of tumor tissue will be collected, if patient has received surgery during hospitalization. Concerning bladder tumor patients only.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • bladder tumor confirmed by cystoscopy and radiology

  • women of childbearing age with negative urine pregnancy test result

  • willing to participate in this trial and sign the informed consent form

Exclusion Criteria:
  • patient with 1) uncontrollable urinary tract infection; 2) severe systemic disease; 3) history of malignancy within the past 5 years; 4) pregnancy or lactation

  • patient involved in other clinical trials

  • other situations researcher considered to be ineligible for this trial

Contacts and Locations

Locations

Site City State Country Postal Code
1 First Affiliated Hospital of Xian Jiaotong University Xi'an Shaanxi China 710061

Sponsors and Collaborators

  • First Affiliated Hospital Xi'an Jiaotong University

Investigators

  • Study Director: Jinhai Fan, MD, First affiliated hospital of Xian jiaotong university

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
First Affiliated Hospital Xi'an Jiaotong University
ClinicalTrials.gov Identifier:
NCT05671289
Other Study ID Numbers:
  • XJTU1AF2022LSL-004
First Posted:
Jan 4, 2023
Last Update Posted:
Jan 12, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by First Affiliated Hospital Xi'an Jiaotong University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 12, 2023