← Back to Clinical Trials
Recruiting NCT07246213

NCT07246213 CAYA Cancer Retrospective Cohort Study

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07246213
Status Recruiting
Phase
Sponsor Resonance, Inc.
Condition Acute Lymphoblastic Leukemia
Study Type OBSERVATIONAL
Enrollment 18,000 participants
Start Date 2025-06-04
Primary Completion 2028-06-04

Eligibility & Interventions

Sex All sexes
Min Age 0 Years
Max Age 21 Years
Study Type OBSERVATIONAL
Interventions
Retrospective Medical Record Review

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 18,000 participants in total. It began in 2025-06-04 with a primary completion date of 2028-06-04.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Despite advances in cancer treatment, significant disparities in outcomes persist between high-income countries (HICs) and low-and middle-income countries (LMICs). Around 80% of children with cancer live in LMICs, where they face challenges such as delayed diagnosis, misdiagnosis, comorbidities, distance to treatment, financial barriers, and limited access to risk-adapted therapies. Acute lymphoblastic leukemia(ALL)/lymphoblastic lymphoma(LBL), for example, is one of the greatest success stories in pediatric oncology, however, such improvements are not evenly distributed worldwide, and the outcomes for leukemia patients are poorer in LMICs compared to HICs, primarily due to reduced access to quality healthcare. This study aims to assess cancer treatment outcomes in LMICs, focusing on acute lymphoblastic leukemia/lymphoblastic lymphoma. The findings will inform future studies to implement evidence-based interventions that improve care quality and reduce treatment failures through targeted strategies.

Eligibility Criteria

Inclusion Criteria: Subjects must meet all the following criteria to be included in this registry: 1. Participants must be willing and able to provide informed consent prior to enrollment in the registry. 1. For minors or individuals unable to provide informed consent, assent must be obtained along with consent from a legal guardian. 2. Note: Exemption applies to this criterion when waiver of informed consent/assent is granted by Institutional Review Board(IRB)/Independent Ethics Committee(IEC)/Competent Authorities(CAs). 2. A confirmed diagnosis of any type of cancer within the 15 years prior to the site's activation date. 3. Age 0 to 21 years at the time of diagnosis. 4. Received substantial anti-cancer treatment at the participating center, including but not limited to: 1. Chemotherapy 2. Surgery 3. Radiation therapy 4. Immunotherapy 5. Medical records are available and accessible for review Exclusion Criteria: * Subjects meeting any of the following criteria will be excluded from this registry: 1. Patients who only visited the participating center for: 1. Consultation without subsequent primary anti-cancer treatment at the participating center 2. Pathology, radiology, or other diagnostic evaluations without treatment

Contact & Investigator

Central Contact

Gabriela Villanueva, MD.

✉ gabriela.villanueva@resonancehealth.org

📞 +1-901-205-9518

Frequently Asked Questions

Who can join the NCT07246213 clinical trial?

This trial is open to participants of all sexes, aged 0 Years or older, up to 21 Years, studying Acute Lymphoblastic Leukemia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07246213 currently recruiting?

Yes, NCT07246213 is actively recruiting participants. Contact the research team at gabriela.villanueva@resonancehealth.org for enrollment information.

Where is the NCT07246213 trial being conducted?

This trial is being conducted at Yerevan, Armenia, El Salvador, El Salvador, Guatemala City, Guatemala, San Pedro Sula, Honduras and 1 additional location.

Who is sponsoring the NCT07246213 clinical trial?

NCT07246213 is sponsored by Resonance, Inc.. The trial plans to enroll 18,000 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology