Actively Recruiting

Age: 18Years +
FEMALE
NCT06279676

Improvement of Women's Health After Allogeneic Stem Cell Transplantation

Led by Ciusss de L'Est de l'Île de Montréal · Updated on 2026-03-18

100

Participants Needed

1

Research Sites

222 weeks

Total Duration

On this page

Sponsors

C

Ciusss de L'Est de l'Île de Montréal

Lead Sponsor

C

Centre hospitalier de l'Université de Montréal (CHUM)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of this prospective research project is to better understand vulvovaginal cGVHD to improve care of allografted women. The expected outcomes include better knowledge of the incidence and manifestations of vulvovaginal cGVHD, risk factors, response to treatments and impact on sexual health of allotransplanted female patients. The knowledge acquired will allow transplant clinicians to make more precise recommendations for gynecological management of future allografted women.

CONDITIONS

Official Title

Improvement of Women's Health After Allogeneic Stem Cell Transplantation

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged 18 years or older
  • Receiving a first allogeneic hematopoietic stem cell transplant (bone marrow or peripheral blood stem cells) from a related, unrelated, cord blood, or haploidentical donor
  • Transplant performed at CIUSSS-EMTL
  • Ability to communicate in French or English
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • Receiving a second allogeneic stem cell transplant
  • Receiving an autologous transplant
  • Unable to give informed consent
  • Unable to communicate in French or English
  • Any condition that the investigators consider makes participation unsuitable

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CIUSSS de l'Est-de-l'Ile-de-Montréal / Hôpital Maisonneuve-Rosemont

Montreal, Quebec, Canada, H1T 2M4

Actively Recruiting

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Research Team

M

Michel-Olivier Gratton

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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