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Impact and Lived Experience of Parents of a Child With a Large or Giant Congenital Melanocytic Nevus (PANGEA)

C

Central Hospital, Nancy, France

Status

Invitation-only

Conditions

Congenital Melanocytic Nevus
Psychology, Social
Parent
Congenital Melanocytic Nevi

Treatments

Other: No Intervention: Observational Cohort

Study type

Observational

Funder types

Other

Identifiers

NCT06934759
2024PI238

Details and patient eligibility

About

The goal of this observational study is to describe the experiences of parents at the birth of a child with a large or giant congenital melanocytic nevus through semi-structured interviews, and to identify potential intervention strategies to improve their care and support.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged 18 years or older
  • Willing to participate in a semi-structured interview
  • Has received full information about the research and has not objected to participating or to the use of their data
  • Able to understand and speak French
  • Parent of a child under 18 years of age

Exclusion criteria

  • Under 18 years of age
  • Not willing to participate
  • Currently under legal protection (e.g., guardianship or curatorship)
  • Cognitive and/or psychological impairments preventing participation in a semi-structured interview
  • Poor understanding and/or expression of the French language
  • Parent of a child over 18 years of age

Trial design

30 participants in 1 patient group

Children with congenital melanocytic nevus
Treatment:
Other: No Intervention: Observational Cohort

Trial contacts and locations

1

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Central trial contact

Anne-Claire BURSZTEJN, Professor; Camille LAHET, Resident

Data sourced from clinicaltrials.gov

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