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The Correlation Between Luteal Serum Progesterone and Live Birth Rate

The Correlation Between Luteal Serum Progesterone and Live Birth Rate in IVF - a Prospective Cohort Study (LUT-2)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05323513
Enrollment
250
Registered
2022-04-12
Start date
2022-03-10
Completion date
2024-05-01
Last updated
2023-07-06

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

Conditions

Infertility

Brief summary

The study design is an observational cohort study. Level of serum P4 will be collected on day OR+4 as well as on the day of embryo transfer (ET) either day OR+3 or OR+5.

Interventions

None listed

Sponsors

Peter Humaidan
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 41 Years
Healthy volunteers
No

Inclusion criteria

* Signed informed consent * BMI \<35kg/m2

Exclusion criteria

* No fresh embryo transfer * Prior participation in the study

Design outcomes

Primary

MeasureTime frameDescription
Live birth rate in relation to luteal serum progesterone levels on day four and three or five9-24 months after inclusionThe birth of a live born child after gestational week 22+0

Secondary

MeasureTime frameDescription
Pregnancy rate in relation to luteal serum progesterone levels14-16 days after oocyte retrievalSerum Human chorionic gonadotropin\<10 IU/l
Clinical pregnancy rate in relation to luteal serum progesterone levels7-9 weeks after inclusionUltrasound scan detection of intrauterine fetal heartbeat in gestational week 7-9

Countries

Denmark

Contacts

Primary ContactPeter Humaidan, Professor
peter.humaidan@midt.rm.dk78445760

Outcome results

None listed

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