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RecruitingNCT06740929JAdoREUpdated May 12, 2026

Hormonal Management of Heavy Menstrual Bleeding in Adolescents

An observational study in Heavy Menstrual Bleeding and Bleeding Disorder, sponsored by University Hospital, Geneva. Recruiting at 1 site in Switzerland. Open to female participants aged Up to 25 Years. Per ClinicalTrials.gov, last updated 2026-05-12.

Sponsored by University Hospital, Geneva · Observational

From the registry’s dates

  • Started Dec 2024; still recruiting 1 year 10 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
163
Ages
Up to 25 Years
Sex
Female
01

Study summary

The goal of this study is to evaluate whether hormonal medications (such as contraceptive pill, patch, injectable progestins and hormonal intra-uterine device) have similar efficacy at managing heavy menstrual bleeding in adolescents with a bleeding disorder compared to those without. We also aim to assess the quality of life and hemoglobin and iron levels in this population.

Read the detailed description

Adolescents with heavy menstrual bleeding and willing to start a hormonal medication to reduce menstrual flow are included. At baseline and during the study period, questionnaires and blood tests are performed. Adolescents with a bleeding disorder are compared to those without. Follow-up is 1 year.

02

Conditions studied

  • Heavy Menstrual Bleeding
  • Bleeding Disorder

Keywords

  • heavy menstrual bleeding
  • bleeding disorder
  • adolescent
  • contraception
  • menstrual management
03

In context

Menorrhagia

206 studies on the registry are indexed under Menorrhagia; 35 are open to participants now.

This study's planned enrollment of 163 is below the median of 210 across 47 observational studies indexed under Menorrhagia.

Browse Menorrhagia studies →

Lead sponsor

University Hospital, Geneva is the lead sponsor of 379 studies on the registry; 70 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 25 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adolescents and young adults presenting to the gynecology consultation at HUG.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adolescents and young adults aged \< 26yo
  • Presenting to the gynecology consultation at HUG
  • Diagnosed with heavy menstrual bleeding (PBAC > 100)
  • Willing to initiate a hormonal medication to manage heavy menstrual bleeding

Exclusion criteria

Exclusion Criteria:

  • Pregnancy or planning to become pregnant during the study period
  • Already using hormonal medication for menstrual management and/or
  • Known anatomical uterine pathology
  • Using anticoagulant or antiaggregant agents
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
163 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna
06

What researchers measure

Primary outcomes

  1. Percentage of reduction in menstrual blood loss

    Using PBAC (pictorial blood loss assessment chart)

    Time frame: 6 months after hormonal medication initiation

Secondary outcomes

  1. Percentage of reduction in menstrual blood loss

    Using PBAC

    Time frame: 3 months following hormonal medication initiation

  2. Percentage of reduction in menstrual blood loss

    Using PBAC

    Time frame: 12 months after hormonal medication initiation

  3. Quality of life

    QoL (measured by the Pediatric Quality of Life Inventory (PedsQL) for adolescents (13-18 years old) or young adults (19-25 years old)) ; range 0-100 with higher scores representing better quality of life.

    Time frame: at baseline, 3 months, 6 months and 12 months

  4. Hemoglobin and ferritin levels changes

    Blood samples to measure hemoglobin and ferritin

    Time frame: at baseline, 6 months and 12 months

  5. Changes in thrombin generation markers

    Blood sample

    Time frame: at baseline and 6 months

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06740929
Responsible party
Dehlia Moussaoui (Principal investigator, University Hospital, Geneva) — Principal investigator
First posted
Dec 18, 2024
Start date
Dec 17, 2024
Primary completion
Jul 2027 (estimated)
Completion
Dec 2027 (estimated)
Last update
May 12, 2026

Study contacts

Dehlia Moussaoui, MD
Contact
dehlia.moussaoui@hug.ch
+41 22 372 33 87

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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