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Trial · NCT03846544

Double Pick up in Poor Prognosis Women

NCT03846544, Phase 4, Completed, CRG UZ Brussel; results first posted 2024-04-15

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Double Pick up in Poor Prognosis Women. Trials, record NCT03846544. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03846544

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Double Pick up in Poor Prognosis Women
NCT number
NCT03846544
Status
Completed
Phases
Phase 4
Enrollment
48 participants, actual
Lead sponsor
CRG UZ Brussel
Conditions
Fertility Disorders
Interventions
Corifollitoropin alfa (CFA)-double pick up
First posted
2019-02-19
Last updated
2024-05-21
Results first posted
2024-04-15

Source ClinicalTrials.gov

Registered outcomes9

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryNumber of MII Oocytes Retrieved Between the Two Arms1 monthnumber of mature (or metaphase II, MII) oocytes retrieved during oocyte retrieval
SecondaryNumber of Preovulatory Follicles1 monthnumber of follicles ≥11m on the day of final oocyte maturation trigger
SecondaryNumber of Cumulus Oocyte Complexes (COCs) Retrieved1 monthnumber of COCs retrieved at oocyte retrieval
SecondaryNumber of Oocytes Fertilized1 monthnumber of fertilized oocytes at day 1 after oocyte retrieval
SecondaryTotal Number of Available Embryos1 monthnumber of available embryos at day 3 or day 5 after oocyte retrieval, good quality and therefore transferable
SecondaryDuration of Ovarian Stimulation1 monthnumber of days of ovarian stimulation
SecondaryClinical Pregnancy Rates4 monthsclinical pregnancy rate
SecondaryLive Birth Rates12 monthsnumber of live births
SecondaryCumulative Live Birth Rates24 monthsdefined as the first live birth following the transfer of fresh and subsequent frozen-thawed embryos

Outcomes9

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of MII Oocytes Retrieved Between the Two Arms1 monthnumber of oocytesMEAN
SECONDARYNumber of Preovulatory Follicles1 monthnumber of folliclesMEAN
SECONDARYNumber of Cumulus Oocyte Complexes (COCs) Retrieved1 monthnumber of oocytesMEAN
SECONDARYNumber of Oocytes Fertilized1 monthnumber of fertilized oocytesMEAN
SECONDARYTotal Number of Available Embryos1 monthnumber of embryosMEAN
SECONDARYDuration of Ovarian Stimulation1 monthdaysMEAN
SECONDARYClinical Pregnancy Rates4 monthsParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYLive Birth Rates12 monthsParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYCumulative Live Birth Rates24 months

Results by group16

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Number of MII Oocytes Retrieved Between the Two ArmsControl Group4.1Standard Deviation 2.4number of oocytes
Number of MII Oocytes Retrieved Between the Two ArmsDouble Pick up Group3.0Standard Deviation 2.2number of oocytes
Number of Preovulatory FolliclesControl Group5.4Standard Deviation 2.2number of follicles
Number of Preovulatory FolliclesDouble Pick up Group5.0Standard Deviation 1.6number of follicles
Number of Cumulus Oocyte Complexes (COCs) RetrievedControl Group5.3Standard Deviation 2.7number of oocytes
Number of Cumulus Oocyte Complexes (COCs) RetrievedDouble Pick up Group3.3Standard Deviation 2.2number of oocytes
Number of Oocytes FertilizedControl Group3.7Standard Deviation 2.4number of fertilized oocytes
Number of Oocytes FertilizedDouble Pick up Group2.3Standard Deviation 2.0number of fertilized oocytes
Total Number of Available EmbryosControl Group1.5Standard Deviation 0.9number of embryos
Total Number of Available EmbryosDouble Pick up Group1.4Standard Deviation 1.3number of embryos

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDControl Group24
Overall StudySTARTEDDouble Pick up Group24
Overall StudyCOMPLETEDControl Group23
Overall StudyCOMPLETEDDouble Pick up Group23
Overall StudyNOT COMPLETEDControl Group1
Overall StudyNOT COMPLETEDDouble Pick up Group1

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityControl Group024
Total, all-cause mortalityDouble Pick up Group024
Total, other adverse eventsControl Group024
Total, other adverse eventsDouble Pick up Group024
Total, serious adverse eventsControl Group024
Total, serious adverse eventsDouble Pick up Group024

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
38199789DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons4

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
Double Pick up Group vs Control Group: Clinical Pregnancy RatesTrial comparisons
Double Pick up Group vs Control Group: deaths from any causeTrial comparisons
Double Pick up Group vs Control Group: Live Birth RatesTrial comparisons
Double Pick up Group vs Control Group: serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT03846544

GET https://conductscience.org/api/trials/v1/NCT03846544/registered