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Clinical comparison of long acting agonist protocol and short acting agonist protocol of in vitro fertilization and embryo transfer: a randomized controlled trial

Clinical comparison of long acting agonist protocol and short acting agonist protocol: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021266
Enrollment
Unknown
Registered
2019-02-06
Start date
2019-02-05
Completion date
Unknown
Last updated
2019-02-11

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

Conditions

Infertility

Interventions

Group 1:Long acting agonist protocol
Group 2:Short acting agonist protocol

Sponsors

Sichuan Provincial Hospital For Woman and Children
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Patients who recieved IVF-ET in our reproductive center.

Exclusion criteria

Exclusion criteria: 1. BMI=29 or <18.5; 2. Patients recieved controlled ovarian hyperstimulation in three months; 3. Patients with endometriosis, hyperprolactinemia,crine disease or metabolic disease; 4. Patients with the history of ovarian excision or raiotherapy; 5. Chromosomal abnormalities.

Design outcomes

Primary

MeasureTime frame
Clinical pregnancy rate;Numbers of oocytes;—

Secondary

MeasureTime frame
Gonadotropins usage duration;—

Countries

China

Contacts

Public ContactYan Gong

Sichuan Provincial Hospital for Woman and Children

gongyan_496181657@qq.com+86 15208393996

Outcome results

None listed

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