Clinical trial Recruiting at 21 sites Observational Ages 18 and up

ALG Lung Cancer Registry (SAFRO2202)

Official title: Observational Study of the Epidemiological, Clinical, and Diagnostic Profile, Treatment Patterns, and Outcomes of Lung Cancer.

Run by Société Algérienne de Formation et de Recherche en Oncologie · NCT07161882 · Data updated 2026-11-12

This registry will collect medical information from adults in Algeria who have been diagnosed with any type of lung cancer to see patterns in diagnosis, treatment, and outcomes.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment3750 (estimated)
SponsorSociété Algérienne de Formation et de Recherche en Oncologie
Academic / other
Drugs / interventionschemotherapy, immunotherapy
Locations21 sites (Algiers, Algiers Province and 20 other locations)
StatusRecruiting
StartedJune 1, 2025
Main results expectedJune 2027
Study endsDecember 2027
Registry record updatedSeptember 16, 2025
Trial IDNCT07161882 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 or older with a histologically confirmed diagnosis of NSCLC, SCLC, or carcinoid tumor diagnosed at inclusion or within the past 12 months who are fully managed at one of the participating oncology or pulmonology departments and who provide informed consent.

Probably not a fit

Patients under 18, those diagnosed more than 12 months before inclusion, those not managed at a participating center, or those currently enrolled in an interventional clinical trial are not eligible and therefore will not benefit from participation in this registry.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

SAFRO2202 is a prospective, multicenter, non-interventional registry enrolling adults with confirmed lung cancer (NSCLC, SCLC, or carcinoid) who were diagnosed at inclusion or within the prior 12 months. The study runs across 21 public and university hospitals in Algeria and captures data during routine clinical care with no study-specific visits or interventions. Patient data are entered into a secure electronic case report form and include demographics, risk factors (notably smoking), tumor histology, staging, molecular markers (for example EGFR, ALK, PD-L1, KRAS, ROS1), treatments, and outcomes including treatment-related side effects. The registry plans to enroll about 1,500 patients per year over a 30-month period to generate real-world national-level evidence on lung cancer management and outcomes.

Why it matters

Potential benefit: If successful, the registry could improve understanding of how lung cancer is diagnosed and treated across Algeria and guide better resource planning and treatment choices for future patients.

How similar studies have gone: National and regional lung cancer registries have previously provided valuable real-world insights into epidemiology and treatment patterns, though they do not test new therapies directly.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age ≥ 18 years
* Histologically confirmed diagnosis of lung cancer (NSCLC, SCLC, or carcinoid tumor)
* Diagnosed at the time of inclusion or within the 12 previous months
* Fully managed (diagnosis, treatment, and follow-up) in an oncology or pulmonology department of one of the 21 participating public/university hospitals
* Signed informed consent obtained

Exclusion Criteria:

* Prior enrollment in this study
* Participation in an interventional clinical trial

Where it's running

  • Centre Pierre et Marie Curie
    Algiers, Algiers Province, Algeria
    Recruiting
  • Chu Beni Messous - Isaad Hassani
    Algiers, Algiers Province, Algeria
    Recruiting
  • CHU Mohamed Lamine Debaghine - Bab-el-Oued
    Algiers, Algiers Province, Algeria
    Recruiting
  • Chu-Beni Messous - Isaad Hassani
    Algiers, Algiers Province, Algeria
    Recruiting
  • EPH Rouiba
    Algiers, Algiers Province, Algeria
    Recruiting
  • CLCC Annaba
    Annaba, Annaba, Algeria
    Recruiting
Show 15 more locations
  • CLCC Batna
    Batna City, Batna, Algeria
    Recruiting
  • CAC-CHU Frantz Fanon
    Blida, Blida Province, Algeria
    Recruiting
  • CHU- Hôpital Khelil Amrane
    Béjaïa, Béjaia Province, Algeria
    Recruiting
  • CHU Dr Abdesselam Benbadis
    Constantine, Constantine Province, Algeria
    Recruiting
  • EH Didouche Mourad
    Constantine, Constantine Province, Algeria
    Recruiting
  • CLCC Draâ Ben Khedda
    Tizi Ouzou, Draâ Ben Khedda, Algeria
    Recruiting
  • CAC-Laghouat
    Laghouat, Laghouat Province, Algeria
    Recruiting
  • CAC Oran EL HASSI- EMIR ABDELKADER
    Oran, Oran Province, Algeria
    Recruiting
  • CHU Dr. Benaouda Benzerdjeb
    Oran, Oran Province, Algeria
    Recruiting
  • EHS 1er novembre
    Oran, Oran Province, Algeria
    Recruiting
  • CAC- Ouargla
    Ouargla, Ouargla Province, Algeria
    Recruiting
  • CAC El OUED
    El Oued, Oued Souf, Algeria
    Recruiting
  • CAC- Sidi Bel Abbès
    Sidi Bel Abbes, Sidi Bel Abbès Province, Algeria
    Recruiting
  • EPH- Sidi Ghiles
    Tipasa, Sidi Ghiles, Algeria
    Recruiting
  • CAC-Sétif
    Sétif, Sétif Province, Algeria
    Recruiting

Study contacts

  • Principal investigator: Adda BOUNEDJAR, Professor of Medical Oncology — Frantz Fanon University Hospital, Cancer Center (CAC), Blida, Algeria
  • Study coordinator: Louisa ISSIAKHEM LOUNICI, CEO
  • Email: l.issiakhem@cmsolutionsdz.com
  • Phone: +213 770 48 43 36

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.