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Gynaecological Gender-affirming Surgeries

A

Amsterdam UMC, location VUmc

Status

Enrolling

Conditions

Gender Dysphoria

Study type

Observational

Funder types

Other

Identifiers

NCT06098781
2020.332

Details and patient eligibility

About

The goal of this prospective cohort study is to learn about the patient report outcomes after gynaecological gender-affirming surgeries (i.e. hysterectomy, tubectomy, colpectomy) among trans-masculine and non-binary individuals (assigned female at birth).

The main question it aims to answer are:

• What is the experienced effect of gynaecological gender-affirming surgeries

Participants will be asked to fill out a questionaire pre-operatively and 3,9 and 18 months post-operatively.

Enrollment

57 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • assigned female at birth
  • scheduled to undergo gynaecological gender-affirming surgery (i.e. hysterectomy, ovariectomy, tubectomy and/or colpectomy)

Exclusion criteria

  • age below 18 y/o
  • surgery combined with other surgeries (e.g. urethroplasty, metoidioplasty)

Trial contacts and locations

1

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Central trial contact

Norah M van Mello, MD, PhD; Judith AF Huirne, MD, PhD

Data sourced from clinicaltrials.gov

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