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Anti-Müllerian HormoneNCT05858307

Clinical Application of Serum Anti-Müllerian Hormone (AMH) Measurements

An observational study of Anti-Müllerian Hormone and Polycystic Ovarian Syndrome, run by Chinese University of Hong Kong at 1 site in Hong Kong.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This study aims to assess the association of Anti-Müllerian hormone (AMH) with polycystic ovarian syndrome, premature ovarian insufficiency and fertility. The main objectives include the following: 1. To study the level of serum AMH in women with PCOS and to evaluate the utility of serum AMH in the diagnosis of PCOS. Read more about this study

Who is it for?
Ages 10 to 44 years, women only
How many people
300 participants
Where
1 siteHong Kong
Study dates
22 Jun 2022to 31 Dec 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 10 to 44 years
  • Women only
  • No healthy volunteers
  • Child, Adult

Study population: The following clients will be included in our study population. * Women attending the Paediatric and Adolescent Gynaecological Clinic and Gynaecological Endocrine Clinic of in the Department of Obstetrics and Gynaecology at the Prince of Wales Hospital for the management of PCOS and POI * Women attending the Assisted Reproductive Technology (ART) Unit of The Chinese University of Hong Kong for ART treatment

Who may be able to join

  • Women attending the Paediatric and Adolescent Gynaecological Clinic and Gynaecological Endocrine Clinic of in the Department of Obstetrics and Gynaecology at the Prince of Wales Hospital for the management of PCOS and POI
  • Women attending the Assisted Reproductive Technology (ART) Unit of The Chinese University of Hong Kong for ART treatment

Who cannot join

  • Women with age <10 or ≥45
  • Current or past diseases affecting gonadotropin, sex steroid secretion, clearance and excretion

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

PUI WAH JACQUELINE CHUNG contact

+852 35051537

jacquelinechung@cuhk.edu.hk

Hong Kong1 site, 1 recruiting
  • The Chinese University of Hong Kong

    Hong Kong

    PUI WAH JACQUELINE CHUNG, MBBS, +852 35051537, jacquelinechung@cuhk.edu.hk

    WING IU LI, +852 35051764, wingiuli@cuhk.edu.hk

    Recruiting

Other trials in Hong Kong

About this study

This study aims to assess the association of Anti-Müllerian hormone (AMH) with polycystic ovarian syndrome, premature ovarian insufficiency and fertility. The main objectives include the following:

  1. To study the level of serum AMH in women with PCOS and to evaluate the utility of serum AMH in the diagnosis of PCOS.
  2. To evaluate the level of serum AMH in women with POI and to evaluate the utility of serum AMH in the management of POI.
  3. To evaluate the associations of basal AMH level with FSH level and AFC respectively for women undergoing ART treatment.
  4. To determine the optimal regimen of gonadotropin for ovarian stimulation for women undergoing ART treatment.
  5. To evaluate the predictive value of serum AMH in reproductive outcomes including oocyte quality, embryo quality, pregnancy loss, clinical pregnancy and live birth rate in women undergoing ART treatment.
Read the detailed description

[Background] Anti-Müllerian hormone (AMH), which level can be assessed in serum, is a product of follicular granulosa cells of preantral and small antral follicles in the ovary. AMH expression increases prior to follicle-stimulating hormone (FSH)-dependent selection (follicles up to 8 mm) and rapidly decreases thereafter (follicles > 8 mm. Thus, serum AMH level is a reliable marker of functional ovarian reserve as it reflects the pool of growing follicles. Since AMH is relatively cycle independent and has no inter-rater variability, it is considered to be a more reliable biomarker of ovarian function across an array of clinical conditions when compared with follicle-stimulating hormone (FSH) and antral follicular count (AFC).

<Association between AMH and polycystic ovarian syndrome (PCOS)> PCOS is a common endocrine disorder that causes menstrual irregularity and hyperandrogenism in women. It affects approximately 4-20% of women of reproductive age. Women with PCOS have been shown to have elevated AMH levels when compared with women without PCOS as there is an increased number of ovarian follicles in PCOS. Therefore, AMH is being increasingly recognised as a marker for the diagnosis of PCOS. However, a specific cutoff value is yet to be determined. When the issue is addressed, serum AMH levels could potentially replace ultrasound in the diagnosis of PCOS as ultrasound is more costly and less accessible.

<Association between AMH and premature ovarian insufficiency (POI)> POI is defined as the cessation of ovarian function before the age of 40 years. Timely diagnosis is important in order to appropriately counsel and treat the patients with POI.

Prompt initiation of hormone replacement therapy is vital to minimise the risk of long-term health complications including osteoporosis and premature cardiovascular disease. AMH levels were significantly low to undetectable in women with POI. Since AMH is independent of the timing in a menstrual cycle, the measurement may be beneficial in the phase of menstrual irregularity and could potentially help to assess the progression of ovarian senescence.

<Associations between AMH and Fertility> Serum AMH level is an important indicator of women's ovarian reserve and a crucial tool in assisted reproductive technology (ART) for the evaluation of women's fertility. A recent systematic review concluded that basal serum AMH is a strong pretreatment predictor of poor response to controlled ovarian stimulation (COS) and correlates with the risk of ovarian hyperstimulation syndrome. As such, clinicians can individualise the stimulation protocols to optimise the ovarian response. In addition, AMH-based prognostication counselling can be provided to patients with realistic expectation regarding the ART outcomes.

Ovarian reserve has a well-established positive correlation with pregnancy outcome. However, current evidence of AMH in the prediction of reproductive outcome following ART treatment remains controversial. Therefore, there is a need to study the predictive value of AMH on pregnancy outcome in women undergoing ART.

[Hypothesis]

  1. Serum AMH level is elevated in women with PCOS.
  2. Serum AMH level is very low or undetectable in women with POI.
  3. Serum AMH level has a significant correlation with FSH and AFC in women undergoing ART treatment.
  4. Serum AMH level can predict reproductive outcomes following ART treatment.

[Study design] This is a prospective observational study.

[Methods] Investigators will collect data from patients who undergo management for PCOS and POI in the Department of Obstetrics and Gynaecology at the Prince of Wales Hospital from 2022 to 2026. For patients undergoing investigation of PCOS and POI, routine venous blood tests for AMH and hormonal profile including FSH, luteinizing hormonal (LH), oestradiol (E2) levels will be obtained. For patients undergoing ART treatment, routine venous blood tests for AMH and hormonal profile, and transvaginal ultrasound for AFC will be arranged to assess the patients' ovarian reserve prior to the commencement of treatment. Patients will be recruited and consent will be obtained for the storage of any remaining serum from the blood tests. The stored blood samples will then be retrieved for this study.

[Data processing and analysis] Data analysis will be performed using the Statistical Packages of Social Sciences for Windows (SPSS, Inc). Data will be presented by percentage, mean and standard deviation, and median where appropriate. Comparisons between groups will be carried out by Student T test/Mann-Whitney U test for continuous variables and Chi-square/Fisher's exact test for categorical data. Two-tailed P<0.05 will be considered significant.

[Sample size] All patients fulfilling the inclusion criteria attending the Department of Obstetrics and Gynaecology at the Prince of Wales Hospital from 2022 to 2026 will be recruited. The sociodemographic records of the participants including their menstrual history, routine hormonal results, ovarian reserve assessment and ultrasound assessment of AFC will be obtained. Metabolic screening results and ART treatment records and subsequent laboratory and reproductive outcome will be obtained if necessary.

Keywords
Anti-Müllerian hormone, Polycystic Ovarian Syndrome, Premature Ovarian Insufficiency, Assisted Reproductive Technology treatment, Predictive value, Reproductive outcomes, AMH, PCOS, POI
Medical subject headings
Polycystic Ovary Syndrome, Primary Ovarian Insufficiency, Infertility

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Serum anti-Müllerian hormone (AMH) (pmol/L)

    To evaluate the serum AMH level of women who undergo investigation for polycystic ovarian syndrome (PCOS), premature ovarian insufficiency (POI) or subfertility

    Measured: Within 1 to 2 months after the day of recruitment

Secondary outcomes (9)
  1. Type of gonadotropin used for ovarian stimulation

    To assess the type of gonadotropin used for ovarian stimulation for women undergoing ART treatment

    Measured: From the first 1 day to last 1 day of ovarian stimulation during ART treatment

  2. Total gonadotropin dose used for ovarian stimulation

    To assess the total gonadotropin dose used for ovarian stimulation for women undergoing ART treatment

    Measured: On the last 1 day of ovarian stimulation during ART treatment

  3. Number of oocytes retrieved

    To evaluate the number of oocytes retrieved during oocyte retrieval for women undergoing ART treatment

    Measured: On the 1 day of oocyte retrieval during ART treatment

  4. Serum follicle stimulation hormone (FSH) (IU/L)

    To evaluate the serum FSH level of women who undergo ART treatment

    Measured: On the first 1 day of ovarian stimulation during ART treatment

  5. Serum luteinising hormone (LH) (IU/L)

    To evaluate the serum LH level of women who undergo ART treatment

    Measured: On the first 1 day of ovarian stimulation during ART treatment

  6. Serum estradiol (pmol/L)

    To evaluate the serum estradiol level of women who undergo ART treatment

    Measured: On the first 1 day of ovarian stimulation during ART treatment

  7. Antral follicle count (AFC)

    To evaluate the AFC of women who undergo ART treatment

    Measured: On the first 1 to 4 days of ovarian stimulation during ART treatment

  8. Clinical pregnancy rate

    To assess for the presence of gestational sac using ultrasonography after embryo transfer procedure for women undergoing ART treatment

    Measured: 6 to 7 weeks of gestation

  9. Live birth rate

    To assess whether live babies are born after women receive ART treatment

    Measured: from 24 weeks of gestation up to 40 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 May 2023
  2. Study start22 Jun 2022
  3. Primary completion30 Jun 2026 (estimated)
  4. Study completion31 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05858307
Sponsor's protocol ID
2022.228
Status last verified
Mar 2025
First submitted
6 Feb 2023
Last updated
27 Mar 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Anti-Müllerian Hormone and Polycystic Ovarian Syndrome, run by Chinese University of Hong Kong at 1 site in Hong Kong.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 27 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact WING IU LI (+852 35051764, wingiuli@cuhk.edu.hk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Serum anti-Müllerian hormone (AMH) (pmol/L) (time frame: Within 1 to 2 months after the day of recruitment). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Mar 2025.

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