ClinicalTrials.gg
RecruitingNCT07481110ECLIPSE-CGUpdated Mar 27, 2026

Study of the Epidemiological, Clinical, Diagnostic, and Therapeutic Characteristics of Gastric Cancers in Algeria

An observational study in Gastric Cancer, Gastric (Stomach) Cancer and Gastric Cancer (Diagnosis), sponsored by Société Algérienne de Formation et Recherche en Oncologie. Recruiting at 15 sites in Algeria. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2026-03-27.

Sponsored by Société Algérienne de Formation et Recherche en Oncologie · Observational

From the registry’s dates

  • Primary completion was expected by Aug 2026, 3 months ago, but the record still lists the study as recruiting.
  • Started Aug 2025; still recruiting 1 year 3 months later.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
1,000
Ages
19 Years and older
Sex
All
01

Study summary

The goal of this observational study is to describe the demographic, epidemiological, clinical, and outcome characteristics of patients with gastric cancer.

It also aims to analyze the diagnostic approaches and management strategies used in the care of these patients in Algeria.

Read the detailed description

This is a non-interventional, observational, descriptive, cross-sectional clinical study with both prospective and retrospective data collection. It aims to describe the demographic, epidemiological, clinical, and outcome characteristics of approximately 1,000 patients with histologically confirmed gastric cancer in Algeria, and to analyze diagnostic and treatment practices.

Data will be collected from medical records and brief patient interviews (≈30 minutes). All information will be anonymized and used exclusively for research purposes.

02

Conditions studied

  • Gastric Cancer
  • Gastric (Stomach) Cancer
  • Gastric Cancer (Diagnosis)

Keywords

  • Gastric Cancer
  • Gastric cancer in Algerian patients
  • Observational study
  • Patient outcomes
  • Oncology
  • Retrospective data
  • Treatment strategies
  • Diagnostic approaches
  • Clinical characteristics
  • Epidemiological data
  • Demographic data
  • Cross-sectional study
  • Real-world data
  • Algeria
  • Algerian Study
03

In context

Stomach Neoplasms

3,399 studies on the registry are indexed under Stomach Neoplasms; 992 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 278 across 790 observational studies indexed under Stomach Neoplasms.

Browse Stomach Neoplasms studies →

Lead sponsor

Société Algérienne de Formation et Recherche en Oncologie is the lead sponsor of 3 studies on the registry; 3 are open to participants now.

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

04

Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with histologically confirmed gastric cancer, followed in the participating oncology departments.

Eligibility criteria

Inclusion Criteria:

  • Patients aged 19 years and older
  • confirmed diagnosis of gastric cancer
  • Patients followed in the participating oncology departments
  • obtained

Non Inclusion Criteria:

  • Histological types other than carcinoma (e.g., GIST, lymphoma, sarcoma, etc.).
  • Secondary gastric tumors
  • Participation in an interventional study
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Histologically or cytologically confirmed

The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).

Your pathology report is the document that shows this.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
1,000 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Demographic characteristics of patients with gastric cancer in Algeria

    The patient's demographic profile will include age (years) and sex. Body Mass Index (BMI) will be calculated using weight (kg) and height (m) according to the formula BMI = weight / height² (kg/m²).

    Time frame: At Baseline ( Initial visit )

  2. Sociological characteristics of patients with gastric cancer in Algeria

    The patient's sociological profile will be described as a composite variable : Education level (primary, secondary, university, other), Profession (employed, unemployed, retired, student, other), Place of residence (current residence; urban or rural), Origin (wilaya of birth/origin)

    Time frame: At Baseline ( Initial visit )

  3. Epidemiological characteristics of patients with gastric cancer in Algeria.

    Frequency (%) of epidemiological risk factors including family history of cancer, Helicobacter pylori infection, smoking status, alcohol consumption, dietary habits, and exposure to chemical substances.

    Time frame: At Baseline (Initial Visit)

  4. Clinical characteristics of patients with gastric cancer in Algeria.

    Distribution of patients according to initial symptoms, tumor localization, histological characteristics, biomarker expression, presence of metastases, and tumor stage according to the AJCC classification.

    Time frame: At Basline ( Initial Visit)

  5. Evolutionary characteristics of patients with gastric cancer.

    Distribution of treatment modalities including surgery (palliative or curative) and chemotherapy (adjuvant or treatment lines), as well as treatment response, complications, disease-free survival (DFS), and duration of response.

    Time frame: At Baseline ( Initial Visit)

Secondary outcomes

  1. Diagnostic modalities in patients with gastric cancer in Algeria

    Proportion (%) of patients diagnosed using endoscopy, biopsy, or imaging, and median time to diagnosis (days) defined as the interval between first reported symptom and confirmed diagnosis.

    Time frame: At Basline (Initial Visit)

  2. Therapeutic management modalities

    Proportion (%) of patients receiving surgery, chemotherapy, targeted therapy, immunotherapy, or palliative care, median time from confirmed diagnosis to initiation of first treatment (days), and proportion of patients with documented post-treatment follow-up.

    Time frame: At Baseline (Initial Visit)

07

Study locations

1 of 15 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Aug 2025 (actual). Primary completion is estimated for Aug 2026, 12 months after the start.

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

Registered
Sep 4, 2025
First posted
Mar 18, 2026
StartActual
Aug 5, 2025
Primary completionEst.
Aug 5, 2026
CompletionEst.
Aug 5, 2026
Last update
Mar 27, 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 Mar 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07481110
Lead sponsor
Société Algérienne de Formation et Recherche en Oncologie
Collaborators
Bristol-Myers Squibb, ES Clinical Research
Responsible party
Sponsor
First posted
Mar 18, 2026
Start date
Aug 5, 2025
Primary completion
Aug 5, 2026 (estimated)
Completion
Aug 5, 2026 (estimated)
Last update
Mar 27, 2026

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

No contact was published for this record. The registry link below has the sponsor’s details.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion