The effect of FSH administration at the time of triggering ovulation with HCG on the outcome of IVF/ICSI

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-12002246

Enrollment

Unknown

Registered

2012-05-20

Start date

2012-06-10

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

infertility

Interventions

group A:give FSH with the dose of 450 IU at the time of triggering ovulation with HCG

group B:give placebo with dose of 450 IU at the time of triggering ovulation with HCG

Eligibility

Sex/Gender

Female

Age

20 Years to 42 Years

Inclusion criteria

Inclusion criteria: 1. women undergoing long protocol IVF/ICSI; 2. age <=42 years old; 3. BMI level between 17-28 kg/m2; 4. basel FSH level <=12 IU/L; 5. women having more than 2 follilces with the diameter no less than 18 mm on the day of HCG administration.

Exclusion criteria

Exclusion criteria: 1. women suffered from recuccent implantation failure (failure to achieve a pregnancy after three or more IVF/ICSI cycles); 2. Submucosalfibroids, intrauterine adhesion, congenitaluterinemalformationsuterine; 3. hydrosalpinx; 4. ovarian endometriomas > 3 cm diameter.

Design outcomes

Primary

Measure	Time frame
clinical pregnancy rate;	—

Secondary

Measure	Time frame
FSH level on the day of oocyte pick up;number of retrieved oocytes;number of mature oocytes;fertilization rate;number of embryos obtained;Ongoing pregnancy rate;Ongoing pregnancy rate;miscarriage rate;	—

Countries

China

Contacts

Public ContactZhang Qingxue

zhangqingxue666@yahoo.cn+86 13602797433

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 18, 2026