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NCT06257888: NAVIMOZ

A Prospective Cohort With Patient Navigation as an Intervention for Breast Cancer Patients

Completed Last updated 11 September 2025
What this trial tests

trial testing patient navigation in Breast Neoplasm Malignant Primary in 90 participants. Completed in 1 May 2025.

Timeline
1 March 2024
Primary endpoint
1 April 2025
1 May 2025

Quick facts

Lead sponsorRenato Cagnacci Neto
StatusCompleted
Study typeOBSERVATIONAL
Enrollment90
Start date1 March 2024
Primary completion1 April 2025
Estimated completion1 May 2025
Sites1 location across Mozambique

Drugs / interventions tested

Conditions studied

Sponsor

Renato Cagnacci Neto

Who can join

18 and older, female only, with Breast Neoplasm Malignant Primary. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this observational study is to introduce a patient navigation system within the breast cancer unit at Hospital Central de Maputo (MOZ) and gather data to assess the efficacy of patient navigation in enhancing oncological outcomes among this patient cohort. The primary inquiries it seeks to address are as follows: * Can patient navigation reduce the duration (in days) between patient admission and the commencement of treatment? * Does patient navigation influence overall survival rates when juxtaposed with historical cohorts from the local setting? Participants will receive continuous support from a patient navigator starting from admission until the initiation of any oncological treatment.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Breast Neoplasm Malignant Primary

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06257888.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing