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CompletedNCT07744477Updated Aug 4, 2026

Validation of Serum Metabolite Differences in Patients With Gallstones and Gallbladder Cancer

An observational study in Gallstone Disease and Gallbladder Malignant Neoplasm, sponsored by Centre Paul Strauss. Completed at 33 sites in 4 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-04.

Sponsored by Centre Paul Strauss · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
230
Ages
18 Years and older
Sex
All
01

Study summary

We have observed that the serum levels of certain metabolites differ between Chilean patients with gallbladder cancer and those with gallstone disease. Based on these discovery results, we selected ten candidate metabolites based on the smallest p-values among metabolites exhibiting a fold-change greater than 1.5. The aim of the present study is to validate these ten differential metabolite levels in an independent cohort of Chilean patients with gallbladder cancer and gallstone disease, and to assess the transferability of these findings to other patient populations.

Read the detailed description

Gallbladder cancer (GBC) is a highly lethal malignant tumour characterized by a low global incidence but a high prevalence in specific populations, particularly in South America. The absence of specific symptoms and validated early detection tools often leads to late diagnosis and poor prognosis. Although altered metabolomic profiles have been described in GBC, and several metabolites have been proposed as potential risk biomarkers, these findings remain largely exploratory and lack consistent validation in independent cohorts, particularly populations with a high incidence of GBC.

Metabolomics provides a comprehensive approach to characterising disease-associated metabolic alterations. Serum metabolites may reflect cancer-related changes in lipid metabolism, bile acid metabolism, amino acid metabolism, and other biological pathways involved in inflammation, carcinogenesis, and tumour progression.

In our previous research, we used the Biocrates platform to obtain serum metabolomics data for 197 Chilean patients, including 86 patients with gallbladder cancer and 111 patients with gallstone disease. The concentrations in serum of more than 1,000 metabolites were processed applying predefined quality-control steps, missing-value filtering, imputation, log2 transformation, and quantile normalisation.

After robust Huber linear regression analysis adjusted for age and sex, the ten metabolites listed below showed the smallest p-values for association with disease status (GBC versus gallstone disease) and a fold-change greater than 1.5. These metabolites have been selected for subsequent validation in the present study:

  1. GCA
  2. TCDCA
  3. GCDCA
  4. PG_16:0_20:3
  5. PE_44:11
  6. PG_16:0_20:4
  7. Cer_d18:1/24:1
  8. Cer_d18:1/16:0
  9. PC_32:0
  10. Cer_d18:1/18:0

The primary aim of this study is to validate the differential serum levels of these ten candidate metabolites in an independent Chilean validation cohort comprising 83 patients with GBC and 82 patients with gallstone disease. In addition, we will assess the transferability of these findings to other populations, including a Peruvian cohort with 32 GBC and 26 gallstone disease patients.

Serum metabolite levels will be quantified using Biocrates XL 500 kit and epidemiological and metabolite data will be analysed in R. Global metabolomic profiles will be explored using principal component analysis to identify samples with atypical metabolic patterns, and the final dataset will be analysed following quality control, log2 transformation, and quantile normalisation.

To validate the ten associations previously identified, serum metabolite levels will be compared between patients with GBC and those with gallstone disease in the independent Chilean validation cohort. Statistical analyses will include linear regression using the rlm function from the MASS R package with a Huber tuning constant of k=1.345, adjusted for age (continuous) and sex (binary covariate). P-values will be corrected for multiple testing using the Bonferroni method. The diagnostic performance of metabolites with validated differential levels will be assessed using receiver operating characteristic (ROC) curve analysis, including area under the curve (AUC), sensitivity, and specificity). Similar analyses will be performed to assess the transferability of serum metabolite differences to other patient populations, e.g. Peruvians.

02

Conditions studied

  • Gallstone Disease
  • Gallbladder Malignant Neoplasm

Keywords

  • Gallbladder cancer
  • Gallstone disease
  • Serum metabolomics
  • Biocrates
  • Biomarker validation
  • South America
  • Chile
  • Peru
  • Bolivia
03

In context

Cholelithiasis

189 studies on the registry are indexed under Cholelithiasis; 42 are open to participants now.

This study's enrollment of 230 is above the median of 197 across 50 observational studies indexed under Cholelithiasis.

Browse Cholelithiasis studies →

Lead sponsor

Centre Paul Strauss is the lead sponsor of 31 studies on the registry; 21 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients with gallstones and cancer-free OR - Patients with gallbladder cancer

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients with gallstones and cancer-free OR - Patients with gallbladder cancer
  • Patients aged 18 years or older

Exclusion criteria

Exclusion Criteria:

  • Patients younger than 18 years
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
230 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Patients diagnosed with gallbladder cancer.

    Other: serum samples

  • Patients with gallstone disease and no evidence of gallbladder cancer upon pathological examination

    Other: serum samples

Interventions

  • Otherserum samples

    serum samples

06

What researchers measure

Primary outcomes

  1. Serum concentrations of five minerals among South American gallstone patients with and without gallbladder cancer

    Time frame: At iclusion

07

Study locations

33 sites
  • Complejo Hospitalario Viedma
    Cochabamba, Bolivia
  • Hospital del Norte
    Cochabamba, Bolivia
  • Hospital Obrero No. 2 (Caja Nacional del Seguro Social)
    Cochabamba, Bolivia
  • Instituto Gastroenterológico
    Cochabamba, Bolivia
  • Instituto Oncológico Nacional
    Cochabamba, Bolivia
  • Hospital Clínico de Magallanes
    Arica, Chile
  • Hospital Regional de Arica
    Arica, Chile
  • Hospital Regional de Concepción,
    Concepción, Chile
  • Hospital De Puerto Montt
    Port Montt, Chile
  • Hospital Regional de Rancagua
    Rancagua, Chile
  • Clínica Alemana de Santiago
    Santiago, Chile
  • Fundación Arturo López Perez (FALP)
    Santiago, Chile
  • Hospital Barros Luco
    Santiago, Chile
  • Hospital Clínico Universidad de Chile
    Santiago, Chile
  • Hospital del Salvador
    Santiago, Chile
  • Hospital El Pino
    Santiago, Chile
  • Hospital Padre Hurtado
    Santiago, Chile
  • Hospital San Borja
    Santiago, Chile
  • Hospital San Juan de Dios
    Santiago, Chile
  • Hospital Sótero del Río
    Santiago, Chile
  • Hospital Regional de Talca
    Talca, Chile
  • Clínica Alemana de Temuco
    Temuco, Chile
  • Complejo Asistencial Padre Las Casas
    Temuco, Chile
  • Hospital Regional de Temuco
    Temuco, Chile
  • Statistical Genetics Research Group, Institute of Medical Biometry, University of Heidelberg
    Heidelberg, Germany
  • Hospital Goyoneche
    Arequipa, Peru
  • Hospital Honorio Delgado
    Arequipa, Peru
  • Instituto Regional de Enfermedades Neoplásicas del Sur (IREN Sur)
    Arequipa, Peru
  • Clínica Monte Sinaí
    Juliaca, Peru
  • Hospital Base III- La Capilla ESSALUD
    Juliaca, Peru
  • Instituto Nacional de Enfermedades Neoplásicas (INEN)
    Lima, Peru
  • Hospital Regional Manuel Nuñez Butrón
    Puno, Peru
  • Instituto Regional de Enfermedades Neoplásicas del Norte (IREN Norte)
    Trujillo, Peru
08

References and documents

Related links

Individual participant data

Plan to share: Yes — Unidentifiable patient data will be deposited in a public data repository after publication, data accession numbers will be provided in the article and upon request.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Dec 2019 to primary completion in Jan 2026, 73 months.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 29, 2026
First posted
Aug 4, 2026
StartActual
Dec 1, 2019
Primary completionActual
Jan 31, 2026
CompletionActual
Jan 31, 2026
Last update
Aug 4, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07744477
Lead sponsor
Centre Paul Strauss
Responsible party
Sponsor
First posted
Aug 4, 2026
Start date
Dec 1, 2019
Primary completion
Jan 31, 2026
Completion
Jan 31, 2026
Last update
Aug 4, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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