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the clinical outcome of CC and MPA in minimal stimulation for poor responders

the clinical outcome of CC and MPA in minimal stimulation for poor responders

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15006430
Enrollment
Unknown
Registered
2015-05-06
Start date
2015-05-11
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

MPA group:MPA oral 10mg/d
MPA+CC group :MPA+CC

Sponsors

Shanghai Nineth people's hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
23 Years to 42 Years

Inclusion criteria

Inclusion criteria: 1. age 25-45 years and the patients have spontaneous menstrual cycle (21-35days); 2. the antral follicle counts are less than 7 in bilateral ovaries on menstrual cycle day 3 or basal serum FSH concentration is no more than 15 mIU/ml; 3. no more than 3 oocytes retrieved in previous classical IVF protocols; 4. no functional cysts present on bilateral ovaries on menstrual cycle day 3.

Exclusion criteria

Exclusion criteria: 1. clinically significant systemic disease such as renal failure; 2. documented ovarian failure; 3. endometriosis grade 3 or higher; or 4. any contraindications to ovarian stimulation treatment.

Design outcomes

Primary

MeasureTime frame
the number of oocyte retrieved;

Secondary

MeasureTime frame
the number of viable embryos;incidence of premature LH;LH value;

Countries

China

Contacts

Public ContactKuang Yanping
kuangyanp@126.com+86 021-53078108

Outcome results

None listed

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