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Antimullerian Hormone as an Indicator for Ovarian Response

Antimullerian Hormone as an Indicator fo Ovarian Response in Women Receiving Long GnRH Agonist Protocol in Intracytoplasmic Sperm Injection Cycles

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03291860
Enrollment
66
Registered
2017-09-25
Start date
2017-11-10
Completion date
2018-10-10
Last updated
2017-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility, Female

Brief summary

Anti Mullerian hormone (AMH) is gaining place as ovarian marker, chiefly in infertility assistance. Investigators explored its correlation with oocytes retrieval after long GnRH agonist protocol for stimulation, in younger and older infertile population. Methods: This prospective analysis compiled data of 66 females, receiving ICSI treatment from April 2016 to October 2017. Serum FSH, LH, Estadiol, AMH and antral follicle count were assessed. Outcomes were measured as good (5 to 19 oocytes) and bad responders.

Interventions

PROCEDUREOvum retrievum

assessment of oocytes collected by ovum retrievum to evaluate the discriminatory power of the antimullerian hormone in ICSI cycles

Sponsors

Ain Shams Maternity Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

1. Age:20-40 years old 2. BMI:20-40kg/m 3. Normal baseline hormonal profile (on the 2nd day of the cycle) * FSH: 2.5-10.2mlU/ml * LH:1.9-12.5mlU/ml * Estradiol (E2): \<50pg/ml 4. No Endometriosis by laparoscopy 5. No prior ovarian surgery; overectomy, ovariectomy or oophrectomy 6. Female subjects who have at least 1 wash-out cycle (defined as greater than or equal to 30 days since the last dose of clomiphene citrate or gonadotrophin treatment) since the last ART cycle and/or clomiphene citrate or gonadotrophin treatment prior to starting gonadotrophin releasing hormone (GnRH) agonist therapy

Exclusion criteria

* 1\. Age: \<20 or \>40 years old 2. BMI: \<20 or \>40kg/m 3. Female subjects with any contraindication for pregnancy. 4. Female subjects with history of tumors of the hypothalamus & pituitary gland. 5\. Female subjects with history of ovarian, uterine or mammary cancer. 6. Female subjects with history of hypersensitivity to the active substance of the medications used for ovarian stimulation. 7\. Abnormal baseline hormonal profile 8. Endometriosis by laparoscopy 9. Previous ovarian surgery; overectomy, ovariectomy or oophrectomy 10. Female subjects with abnormal gynecological bleeding of unknown etiology

Design outcomes

Primary

MeasureTime frameDescription
Difference between AMH levels between good and poor responders in young patients receiving long GnRH agonist protocol for ICSI.1 month (1 cycle)Measurement of AMH level in patients undergoing controlled ovarian stimulation prior to ICSI using long GnRH agonist protocol. Level will be compared between good and poor responders.

Contacts

Primary ContactAhmed M Selim, MBBCh
dr.ahmedselim_89@yahoo.com00201123122003

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026