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NCT04330066

Impact of Endometrial Compaction in Euploid Frozen Embryo Transfers

Status unknown Last updated 11 March 2022
What this trial tests

trial testing Abdominal ultrasound measurement of the endometrial lining in Infertility, Female in 187 participants. Status unknown.

Timeline
1 September 2020
Primary endpoint
30 May 2022
30 June 2022

Quick facts

Lead sponsorBoston IVF
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment187
Start date1 September 2020
Primary completion30 May 2022
Estimated completion30 June 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Boston IVF

Who can join

Adults 18 to 44, female only, with Infertility, Female. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this pilot study is to evaluate whether a decrease in endometrial thickness (compaction) prior to progesterone exposure (endogenous or exogenous) to the day before a single frozen embryo transfer has an impact on the clinical pregnancy rate with euploid embryos in exogenous hormone and modified natural thaw cycles. Information derived from this study may give insight on ways to improve pregnancy rates in cryo-thaw cycles.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Endometrial compaction does not predict live birth in single euploid frozen embryo transfers: a prospective study.
    Shah JS, Vaughan DA, Dodge LE, Leung A, et al · · 2022 · cited 16× · PMID 35357436 · DOI 10.1093/humrep/deac060

Verify or expand the search:

Other recruiting trials for Infertility, Female

Currently open trials in the same condition.

Other Boston IVF trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04330066.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing