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The effect of selenium and vit E supplementation on Oogenesis improvement in infertile women with occult premature ovarian insufficiency: A randomized contorolled clinical trial

The effect of selenium and vit E supplementation on anti-mullerian hormone (AMH) index and antral follicle count in infertile women with occult premature ovarian insufficiency: A randomized contorolled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160410027311N6
Enrollment
70
Registered
2018-04-30
Start date
2018-05-04
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

occult premature ovarian insufficiency. Primary ovarian failure

Interventions

Intervention 1: Intervention group: The intervention group will receive one tablet of selenium 200 micrograms daily and one vitamin E 400 units per day for 90 days. Intervention 2: Control group: The

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Accepting informed written consent Women aged 20 to 40 years old Menstrual cycle Having two ovaries There is no evidence of endocrine disorders (diabetes, thyroid disorders, Addison's disease, etc.) by asking the patient and checking out the results of previous patient tests. Occult POI (hormone AMH <1 ng / ml, reduced ovarian reserve, less than 5 anthral follicles, reduced ovarian volume to less than 2.5 cubic centimeters, or all three cases) With BMI <30, the weight and height in this study will be measured by the researcher and the BMI will be calculated according to the formula below. BMI = (WEIGHT (kg)) / (LENGTH (m ^ 2))

Exclusion criteria

Exclusion criteria: Drug Addiction and Smoking The tendency to use donated eggs Having evidence of OVERT POI (FSH> 15 or amenorrhea for more than 3 months) Supplementation of selenium and vitamin E three months before the onset of intervention Having a history of radiotherapy and chemotherapy The use of anticoagulants (co-administration of vitamin E with these drugs increases the risk of bleeding)

Design outcomes

Primary

MeasureTime frame
Concentration of anti-mullerian hormone (AMH). Timepoint: Before the intervention begins and 12 months after the intervention begins. Method of measurement: To monitor the level of anti-mullerian hormone, blood sampling will be performed on the day of referral from the Brachial vein and will be immediately transferred to the laboratory and will be used with an ELISA kit.;Number of ovarian antal follicles. Timepoint: Before the intervention begins and 12 months after the intervention begins. Method of measurement: Transvaginal ultrasonography of the ovary on the third day of the menstrual cycle, performed by a radiologist and a device for all participants to check the number of antral follicles.

Secondary

MeasureTime frame
Ovarian volume. Timepoint: Before the intervention begins and 12 months after the intervention begins. Method of measurement: Ovarian volume with the same ultrasound on the third day of menstruation using the following formula Ovarian volume = Length × height × width × p / 6 It will be calculated for each ovary separately.;The incidence of side effects of selenium and vitamin E and their placebo. Timepoint: After the end of the intervention. Method of measurement: The side effects of medicines will be questioned according to the checklist given during supplements or placebo and will be recorded in the checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSafiyeh Farhadi Dizaji

Tabriz University of Medical Sciences

s63farhadi@gmail.com+98 41 3479 6770

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026