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PCOSNCT04364087

Glucose Metabolism and Live Birth Outcomes in PCOS

An observational study of PCOS and Infertility, run by Mỹ Đức Hospital at 1 site in Vietnam.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Polycystic ovary syndrome (PCOS) is a common endocrine and reproductive disorder in which insulin resistance (IR) is proposed as a key pathophysiological feature of the disease's symptoms and consequences. Read more about this study

Who is it for?
Ages 18 to 40 years, women only
Conditions the study is for
PCOS, Infertility, Diabetes
What is being tested?
Oral glucose tolerance test
Type of treatment
Pill or oral medicine
How many people
1,208 participants
Where
1 siteVietnam
Study dates
1 Jun 2020to 31 Aug 2022
Phase
Observational
Are there results?
None posted in the registry

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 18 to 40 years
  • Women only
  • No healthy volunteers
  • Adult

Study population: Infertile Vietnamese women aged 18-40 years, diagnosed with polycystic ovary syndrome (PCOS) according to the Rotterdam 2003 criteria, who present for infertility treatment at IVFMD.

Who may be able to join

  • Vietnamese women aged 18-40 years
  • Diagnosed with polycystic ovary syndrome (PCOS) according to the Rotterdam criteria (2003)
  • Having indications for infertility treatment

Who cannot join

  • Thyroid-stimulating hormone (TSH) > 5 mIU/mL
  • Serum prolactin (PRL) > 30 ng/mL
  • History of hypothyroidism
  • Cushing's syndrome
  • Premature ovarian insufficiency
  • Late-onset or non-classic congenital adrenal hyperplasia
  • Any other concomitant endocrinopathy

Trial locations and contacts

1 site in 1 country.

Vietnam1 site
  • My Duc Hospital

    Ho Chi Minh City

Other trials in Vietnam

About this study

Official title: Impact of Glucose Metabolism Abnormalities on Live Birth Rate in South-East Asian Women With Polycystic Ovary Syndrome

Polycystic ovary syndrome (PCOS) is a common endocrine and reproductive disorder in which insulin resistance (IR) is proposed as a key pathophysiological feature of the disease's symptoms and consequences. Diabetes and rediabetes, a significant consequence of IR, are related to a higher risk of diabetes mellitus, future cardiovascular events, and adverse pregnancy outcomes.

Read the detailed description

All Vietnamese infertile women with PCOS, according to the Rotterdam criteria present at IVFMD, will be enrolled in the study. Phenotypes of PCOS are classified into A, B, C, and D due to hyperandrogenism (HA), ovulatory dysfunction (OD), and polycystic ovarian morphology (PCOM)

  • A: HA + OD + PCOM
  • B: HA + OD
  • C: HA + PCOM
  • D: OD + PCOM

All patients enrolled in this study will have:

  • Standard anthropometric data will be done by professional and experienced physicians according to standard study protocol: Weight, height, waist and hip circumference, waist-to-hip ratio, and BMI calculated, followed by World Health Organization guidelines for Asian women. Trained midwives evaluated hirsutism and acanthosis nigricans, and fat mass was measured in the abdomen area using specific calipers (Accu-Measure®).
  • Gynecologic ultrasound scan
  • Blood tests:

A fasting blood sample was obtained. Luteinizing hormone (LH) (with a coefficient of variation [CV] 2.3%), follicle-stimulating hormone (FSH) (CV 3.5%), estradiol (CV 2.7%), progesterone (CV: 6.2%), prolactin (CV: 5.2%), sex hormone binding globulin (SHBG) (CV 5.6%), total testosterone (CV 8.4%) were measured by Elesys technique, Cobas e411 system. FAI was calculated using the formula: FAI = serum testosterone in nmol/L/serum SHBG in nmol/L × 100. Thyroid stimulating hormone (TSH) (CV 6.0%), free thyroxin (fT4) (CV 5.05%) were measured by Access 2 immunoassay system. High-density lipoprotein cholesterol (HDL-C) (CV 2.4%), low-density lipoprotein cholesterol (LDL-C) (CV 2.0%), and triglyceride (CV 1.76%) were measured by Beckman Coulter AU480 system. Fasting serum insulin (CV 2.8%) was measured by Elesys technique, Cobas e411 system. The Homeostasis Model Assessment of Insulin Resistance Index (HOMA-IR) was used to estimate insulin sensitivity. HOMA-IR was calculated as FPG in mmol/L × fasting insulin in mIU/mL/22.5 (Matthews et al., 1985). A 2 mL blood sample was withdrawn and stored in a vacutainer with nature oxalate and EDTA additive.

  • Glucose tests:

+ After a fast of ≥4 hours, FPG (CV 0.9%) was measured by Beckman Coulter AU480 analyzer, and HbA1c (CV 1.00%) were measured by Tosoh HLC-723GX analyzer; participants who had not fasted for ≥4 hours were asked to return for measurement of FPG the next day.

Diagnosis of diabetes mellitus will be made when fasting glucose ≥126 mg/dL (7 nmol/L) or HbA1C ≥6.5% (48 mmol/mol) (American Diabetes Association, 2018). When glucose ≥126 mg/dL (7 nmol/L) or HbA1C ≥6.5% (48 mmol/mol) (American Diabetes Association, 2018).

  • Oral glucose tolerance test with 75 g glucose (75 g OGTT) will be performed on those with normal fasting glucose and HbA1C levels. Women will be recommended to have a normal diet for three days and overnight fasting for at least 8 hours. The blood withdrawal will be performed twice: (i) fasting and (2i) 2 hours after solution administration. The volume of blood for each test is 2 ml. Impaired glucose tolerance will be diagnosed when two-hour glucose levels of 140 to 199 mg/dL (7.8 to 11.0 mmol/l) (American Diabetes Association, 2018).
  • Hyperandrogenism:
  • Clinical hyperandrogenism: Hirsutism using the modified Ferriman Gallwey score (mFG) and severe acne
  • Biochemical hyperandrogenism: free testosterone (normal range below 2,53nmol/ml), free testosterone index, SHBG

Following the assessment of glucose metabolism, all patients identified with preconception glucose metabolism disorders (e.g., prediabetes or diabetes) were referred to endocrinologists for specialized preconception care. This included lifestyle modifications and/or pharmacological interventions, aiming to optimize metabolic health before conception and potentially reduce adverse pregnancy outcome. Conception was achieved through various methods, including natural conception, ovulation induction combined with intrauterine insemination (OI/IUI), or in-vitro fertilization/ in-vitro maturation (IVF/IVM). These treatment options were counseled based on the recommendations from the 2023 international evidence-based guideline, in which first-line therapy involves optimizing preconception health and lifestyle, followed by OI with letrozole. Timed intercourse was recommended in the absence of male factor infertility, while IUI was offered in cases with mild male factor. IVF/IVM was indicated after failure of these initial approaches. Final decisions were individualized through shared decision-making, depending on clinical indications and patient preference (Teede et al., 2023b). Pregnancy outcomes, including pregnancy rates, live births and pregnancy outcomes, were tracked and documented over a 24-month follow-up period from the time of study enrollment.

Being tested
Oral glucose tolerance test
Medical subject headings
Infertility, Diabetes Mellitus, Prediabetic State

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Oral glucose tolerance testDiagnostic test

    Oral glucose tolerance test with 75 g glucose (75 g OGTT) will be performed to those with normal fasting glucose and HbA1C levels. Women will be recommended to have normal diet for 3 days and overnight fasting for at least 8 hours. The blood withdrawal will be performed twice: (i) fasting and (2i) 2 hours after solution administration. The volume of blood for each test is 2 ml. Impaired glucose tolerance will be diagnosed when two-hour glucose levels of 140 to 199 mg/dL (7.8 to 11.0 mmol/l) (American Diabetes Association, 2018).

Study groups in NCT04364087
Study groupRoleWhat they receive
Infertile PCOS womenAll Vietnamese, infertile women, diagnosed with PCOS according to the Rotterdam criteria (2003) at IVFMD Tan Binh and IVFMD Phu Nhuan will be enrolled to the study.
Receives: Diagnostic Test: Oral glucose tolerance test

What is being measured

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

  1. Live birth rate at 24 months following enrollment into the study

    Live birth was defined as the delivery of a live infant after 22 weeks of gestation, regardless of the method of conception.

    Measured: From enrollment until delivery (up to 24 months after enrollment)

Secondary outcomes (9)
  1. Gestational diabetes mellitus

    Diagnosis based on standard criteria recorded in medical records.

    Measured: From enrollment until delivery (up to 24 months after enrollment).

  2. Hypertensive disorders of pregnancy

    Includes gestational hypertension, preeclampsia, and eclampsia.

    Measured: From enrollment until delivery (up to 24 months after enrollment).

  3. Miscarriage

    Pregnancy loss before 22 weeks of gestation.

    Measured: From enrollment until delivery (up to 24 months after enrollment).

  4. Preterm birth

    Delivery before 37 completed weeks of gestation.

    Measured: From enrollment until delivery (up to 24 months after enrollment).

  5. Birthweight

    Neonatal birthweight measured in grams at delivery; categorized as low birthweight (<2500 g) or macrosomia (≥4000 g).

    Measured: At delivery (up to 24 months after enrollment).

  6. Gestational age at birth

    Gestational age in completed weeks at delivery.

    Measured: At delivery (up to 24 months after enrollment).

  7. Neonatal Intensive Care Unit (NICU) admission

    Admission to NICU after birth (yes/no).

    Measured: At delivery (up to 24 months after enrollment).

  8. Neonatal respiratory distress

    Clinical diagnosis of respiratory distress requiring intervention.

    Measured: At delivery (up to 24 months after enrollment).

  9. Baseline glycemic status (diabetes, prediabetes, or normal glucose tolerance before infertility treatment)

    Glycemic status will be determined before initiation of infertility treatment, based on the 75-g oral glucose tolerance test (OGTT), fasting plasma glucose, and HbA1c, according to the American Diabetes Association (ADA) 2023 criteria. Participants will be categorized into: Diabetes mellitus, Prediabetes, Normal glucose tolerance.

    Unit of Measure: Number of participants (%) in each category.

    Measured: At baseline (at enrollment, before treatment).

Timeline

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

  1. First posted27 Apr 2020
  2. Study start1 Jun 2020
  3. Primary completion31 Aug 2022
  4. Study completion31 Aug 2022

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
1,208 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04364087
Sponsor's protocol ID
08/20/ĐĐ-BVMD
Status last verified
Aug 2025
First submitted
24 Apr 2020
Last updated
24 Aug 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Nguyen NT, Ho VNA, Pham TD, Nguyen MHN, Nguyen DL, Le HL, Le KTQ, Ly LD, Tran MTN, Ho TM, Norman RJ, Vuong LN. Impact of glucose metabolism abnormalities on live birth rate in South-East Asian women with polycystic ovary syndrome. Hum Reprod Open. 2026 Feb 17;2026(2):hoag012. doi: 10.1093/hropen/hoag012. eCollection 2026.

    PubMed 41836352

Questions about this trial

What is this clinical trial studying?

An observational study of PCOS and Infertility, run by Mỹ Đức Hospital at 1 site in Vietnam.

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 3 inclusion and 7 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: finished, as of the sponsor's last update on 24 Aug 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 Vietnam. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Live birth rate at 24 months following enrollment into the study (time frame: From enrollment until delivery (up to 24 months after enrollment)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04364087, which also lists 1 linked publication.

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 24 Aug 2025.

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