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A Trial Comparing Qam With Qpm Dosing in Assisted Reproductive Technologies (ART)

A Prospective Randomized Trial Comparing Qam With Qpm Daily Dosing in Assisted Reproductive Technologies

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01139593
Enrollment
128
Registered
2010-06-08
Start date
2010-06-30
Completion date
2015-12-31
Last updated
2015-12-09

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

Conditions

Infertility

Keywords

IVF, ICSI, gonadotropin, am dose, pm dose, pregnancy, implantation, live birth

Brief summary

This is a prospective randomized trial comparing the outcome in women undergoing IVF/ICSI when taking their gonadotropin dosage in the morning (am) or evening (pm).

Interventions

None listed

Sponsors

Virginia Center for Reproductive Medicine
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 42 Years
Healthy volunteers
No

Inclusion criteria

* women between 21-42 undergoing IVF

Exclusion criteria

* women \> 45, * women with one ovary, * donor egg, * surrogacy, * FET cycles, * uterine problems, * large fibroids

Design outcomes

Primary

MeasureTime frame
Live birth rate4 years

Countries

United States

Outcome results

None listed

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