Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02309047
Other study ID # 12-645
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 2004
Est. completion date August 2023

Study information

Verified date October 2021
Source UMC Utrecht
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Through the COLA Study and Biobank the investigators hope to enable further identification of phenotype, endocrine, ethnic, and metabolic characteristics associated with menstrual cycle disturbances; and: the identification of genetic or other etiologic factors associated with cycle disturbances.


Description:

Population Women with cycle disturbances are referred to the outpatient clinic specialized in cycle disturbances by 1st or 2nd line care providers for further diagnostic procedures. Inclusion criteria WHO I Hypogonadotropic hypoestrogenic status (previously: "hypothalamic amenorrhea") 1. Low to normal serum follicle-stimulating hormone (FSH) concentrations 2. Low serum estradiol concentrations WHO II 1. Amenorrhea or oligomenorrhea (mean cycle >35 days during the last 6 months) 2. Normal serum FSH concentrations (<12 IU/L) 3. Absence of other causes for the cycle disturbance, including: normal prolactin concentrations (<1.0 IU/L), normal thyroid stimulating hormone (TSH) concentrations (0.2 - 4.2 milli-International unit /L), abnormalities on ultrasonography. Within women with WHO II status, polycystic ovary syndrome (PCOS) is diagnosed when at least 2 of the following criteria are met: 1. Oligo-/anovulation 2. Clinical and/ or biochemical hyperandrogenism 3. Polycystic ovaries on ultrasonography WHO III 1. primary ovarian insufficiency (POI): defined as secondary amenorrhea before the age of 40 years and basal FSH > 40 IU/L. 2. incipient ovarian failure (IOF): defined as normal-ovulatory cycles with raised basal FSH > 12 IU/L before the age of 40 years. 3. transient ovarian failure (TOF): defined as irregular cycles with raised basal FSH > 12 IU/L before the age of 40 years. 4. Poor ovarian response: defined as less than 4 oocytes retrieved or cancellation in case of absent follicle growth after ovarian hyperstimulation with 300 IU gonadotropins. 5. Early menopause: menopause occurring between age 40 and 45 years. 6. Hypergonadotropic primary amenorrhea: primary amenorrhea with raised basal FSH > 12 IU/L. Controls For analyses in which comparison with female controls are needed, data will be collected from existing population based cohorts, such as the EPIC cohort (Julius Center), or selected women included in the preconceptional cohort (PC, derived from the Department of Reproductive Medicine and Gynaecology in the University Medical Center Utrecht (UMCU), separate protocol in preparation). Exclusion criteria - Age: younger than 18 yrs. - Regularly cycling women, with the exception of women with elevated basal FSH concentrations (IOF cases). Study parameters In order to determine the phenotype characteristics of women with cycle disturbances, and to allow for the identification of genetic factors associated with cycle disturbances, the following parameters will be obtained. - Age - Ethnicity - Social economic status and education - Intoxications: smoking habits (previous and current), use of alcohol or drugs - Medication and medication history - Mental health (depression, stress and anxiety) - Cycle regularity: age at menarche, use of (oral/intrauterine) contraceptives, mean duration of cycle, variation in cycle duration. - Reproductive & obstetric history: parity, time to pregnancy and pregnancy outcome, subfertility (including treatments) - Medical history (including previous gonadotoxic treatment) - Family history of diabetes mellitus, early menopause, cycle irregularities, subfertility, cardiovascular disease, endocrinological disease, congenital disorders - Basic physical examination: systolic and diastolic blood pressure, height, weight (BMI), waist circumference, hip circumference - Assessment of hirsutism, acne, Tanner sexual development stages. - Ovarian reserve parameters: antral follicle count, ovarian volume, anti-müllerian hormone (AMH) - luteinizing hormone (LH), FSH, prolactin, TSH, estradiol concentrations - Androgen levels - Lipid spectrum, glucose, insulin, High sensitivity C-reactive protein - In POI specifically: bone density as assessed by dual-energy X-ray absorptiometry (DEXA), karyotype, fragile X premutation screening, presence of autoantibodies (against thyroid, ovaries, parietal cells and adrenal gland). Participation in the COLA Biobank will consist of the additional withdrawal of two blood vials (one for DNA and one for serum sampling) obtained during the routine diagnostic procedure. Relatives of the index patient: When a familial tendency of the WHO status is suspected on the basis of family history of 1st and 2nd degree relatives, these relatives will be invited for participation of the study.


Recruitment information / eligibility

Status Recruiting
Enrollment 5000
Est. completion date August 2023
Est. primary completion date June 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: WHO I Hypogonadotropic hypoestrogenic status (previously: "hypothalamic amenorrhea") 1. Low to normal serum FSH concentrations 2. Low serum estradiol concentrations WHO II 1. Amenorrhea or oligomenorrhea (mean cycle >35 days during the last 6 months) 2. Normal serum FSH concentrations (<12 IU/L) 3. Absence of other causes for the cycle disturbance, including: normal prolactin concentrations (<1.0 IU/L), normal TSH concentrations (0.2 - 4.2 milliunits/L), abnormalities on ultrasonography. Within women with WHO II status, PCOS is diagnosed when at least 2 of the following criteria are met: 1. Oligo-/anovulation 2. Clinical and/ or biochemical hyperandrogenism 3. Polycystic ovaries on ultrasonography WHO III 1. POI: defined as secondary amenorrhea before the age of 40 years and basal FSH > 40 IU/L. 2. IOF: defined as normal ovulatory cycles with raised basal FSH > 12 IU/L before the age of 40 years. 3. TOF: defined as irregular cycles with raised basal FSH > 12 IU/L before the age of 40 years. 4. Poor ovarian response: defined as less than 4 oocytes retrieved or cancellation in case of absent follicle growth after ovarian hyperstimulation with 300 IU gonadotropins. 5. Early menopause: menopause occurring between age 40 and 45 years. 6. Hypergonadotropic primary amenorrhea: primary amenorrhea with raised basal FSH > 12 IU/L. Exclusion criteria: Exclusion criteria - Age: younger than 18 yrs. - Regularly cycling women, with the exception of women with elevated basal FSH concentrations (IOF cases).

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Netherlands University Medical Center Utrecht Utrecht

Sponsors (1)

Lead Sponsor Collaborator
UMC Utrecht

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary hormonal classification FSH, LH, Estradiol, Progesterone,Testosterone, Androstenedione, Sex hormone binding globulin (SHBG), Cortisol, TSH within 6 weeks
Primary metabolic profile total cholesterol, triglycerides, LDL cholesterol, HDL cholesterol, insulin, glucose within 6 weeks
Primary ovarian reserve anti mullerian hormone, FSH and antral follicle count. within 6 weeks
Secondary autoimmunity in WHO 3- POI patients antithyroid peroxidase, antiadrenal, antiparietal and antiovarian antibodies within 3 months
Secondary bone density in WHO 3- POI patients a dual-energy x-ray absorptiometry (DEXA) scan within 3 months
Secondary genotype in WHO 3 POI patients karotype, fragile X mental retardation 1 gene premutation carriership within 3 months
See also
  Status Clinical Trial Phase
Completed NCT01653743 - Trial to Assess the Clinical Efficacy and Safety of MSJ-0011 in Inducing Ovulation in Anovulatory or Oligo-ovulatory Japanese Women Phase 3
Completed NCT00327366 - Effect of Bright Light on Sex Hormones and Ovulation in Humans N/A
Not yet recruiting NCT02551367 - Letrozole Versus Clomiphene Citrate for Ovulation Induction in Women With Poly Cystic Ovary Syndrome ( PCOS ) Phase 2
Completed NCT01923194 - Evaluation of Efficacy and Safety of Highly Purified Urofollitropin for Ovulation Induction in Chinese Females Phase 3
Completed NCT01008319 - Traditional Clomiphene Citrate Administration vs. Stair-step Approach Phase 3
Completed NCT00239603 - Efficacy Study of the OV-Watch™ Personal Fertility Monitor for Women Using Clomiphene Citrate. Phase 4
Completed NCT03252223 - Ovarian Response to Recombinant Follicle Stimulating Hormone in Women With PCOS Phase 4
Completed NCT00492882 - Study of Mechanisms of Anovulation in Polycystic Ovary Syndrome Phase 4
Completed NCT02335879 - Phase III Clinical Study of Domestic Recombinant Human Follitropin for Injection to Treat WHO Class II Anovulation Phase 3
Completed NCT00471523 - Treatment of Anovulatory Infertility in PCOS Patients Phase 4
Completed NCT02703649 - Administration of Single High Dose Letrozole for Ovulation Induction Phase 4
Completed NCT00213148 - Comparison of Anastrozole Verses Clomiphene Citrate in Stimulating Follicular Growth and Ovulation in Infertile Women With Ovulatory Dysfunction Phase 2
Completed NCT03018314 - Serum Kisspeptin Levels in Infertile Women N/A
Completed NCT02710981 - Sildenafil Vaginal Gel Co-treatment With Clomiphene Citrate in Infertile Women With Thin Endometrium N/A
Recruiting NCT02186782 - Concomitant CC and E2 Versus CC Alone in Ovulation Induction Phase 4
Not yet recruiting NCT00665171 - Whole Genome Analysis for the Detection of Key Genes in the Polycystic Ovary Syndrome N/A
Withdrawn NCT03155828 - Using CPAP to Improve Menstruation in Women With Polycystic Ovarian Syndrome and Obstructive Sleep Apnea
Withdrawn NCT00453219 - FHA: Characterization of Metabolic Status, Brain Circuitry, and Stress-Reactivity N/A
Completed NCT00920634 - Protocol for Drug Use Investigation of Follistim Injection (Study P06132)(COMPLETED)
Recruiting NCT06208995 - Quality of Life in Normogonadotropic Anovulation

External Links