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Study on the Occurrence of Head and Neck Cancers During Pregnancy

Study on the Occurrence of Head and Neck Cancers During Pregnancy

Status
Suspended
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03738267
Acronym
REFCORbirth
Enrollment
14
Registered
2018-11-13
Start date
2018-11-07
Completion date
2025-09-23
Last updated
2025-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Head and Neck Cancer, Pregnancy Related

Brief summary

Head and neck cancers that occurred during pregnancy

Interventions

None listed

Sponsors

French scientific group REFCOR
CollaboratorUNKNOWN
Centre Francois Baclesse
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18 year old woman or over at the time of participation * PS 0 -2 * Cancer diagnosed (biopsy date) from 01/01/2010 between the second week of pregnancy and the 12 months postpartum. * Primitive may concern the following sites: oral cavity, nasopharynx, oropharynx, hypopharynx, larynx, prevalent lymphadenopathy, nasal cavity, salivary glands, dental tumors, ear tumors, paragangliomas optic pathways, facial sinus / facial mass, nose, ear and other head and neck * All histologies (epithelial tumors, sarcomas, mucosal melanomas, embryonic tumors, undifferentiated tumors) * Patient receiving or having received a specific oncological treatment among surgery, radiotherapy, chemotherapy, hormone therapy. * All stages allowed: localized stages and metastatic stages immediately. * No opposition of the patient to participate in this study

Exclusion criteria

* Any other neoplastic antecedent * Exclusion of metastases at the level of the VADS of another primitive than a cancer of the VADS * Exclusion of hematological tumors (lymphoma) and glial tumors * Person subject to a legal protection measure or unable to express their consent

Design outcomes

Primary

MeasureTime frameDescription
Serological status of patientsThrough study completion, an average of 5 yearsNumber of patients with positive or negative serological status for PVH (Papilloma Virus Humain) and EBV (Epstein-Barr Virus)
Characteristics pregnancy of patientsThrough study completion, an average of 5 yearsPresence or absence of maternal-fetal diseases
Tumor characteristics of patientsThrough study completion, an average of 5 yearsHistological type of cancer

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026