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Trial · NCT05173597

Real-world Evidence on Follitropin Delta Individual Dosing

NCT05173597, Recruiting, University of Luebeck

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Real-world Evidence on Follitropin Delta Individual Dosing. Trials, record NCT05173597. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05173597

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Trial

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

Title
Real-world Evidence on Follitropin Delta Individual Dosing
NCT number
NCT05173597
Status
Recruiting
Enrollment
850 participants, estimated
Lead sponsor
University of Luebeck
Conditions
Infertility, Sterility
Interventions
Follitropin delta
First posted
2021-12-30
Last updated
2025-03-30

Source ClinicalTrials.gov

Registered outcomes9

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

ListOutcomeTime frameDescription
PrimaryOvarian response2021-2022
Number of cumulus-oocyte-complexes of the individual dosing regimen of follitropin delta for controlled ovarian stimulation for in-vitro fertilisation (IVF) or intracytoplasmic sperm injection (ICSI) in a cohort of patients from a real-world setting with focus on high body weight.
SecondaryOverall treatment outcome2021-2022Incidence of live birth stratified for low, normal and high AMH and body weight
SecondaryChange in body weight2021-2022Determine change in body weight between 1st and 2nd cycle in subjects undergoing two cycles
SecondaryIncidence of dose changes2021-2022Incidence of dose changes between 1st and 2nd treatment cycle in subjects undergoing two cycles
SecondaryIntra-individual variation of ovarian response2021-2022
Intra-individual variation of the number of cumulus-oocyte-complexes retrieved between 1st and 2nd treatment cycle in subjects undergoing two cycles, stratified for low, normal and high AMH and body weight and cycle regularity
SecondaryMeasurement of correlation of variance of body weight and AMH2021-2022Correlation coefficient of variance of body weight and AMH with variance of ovarian response between 1st and 2nd cycle in subjects undergoing two cycles
SecondaryComparison of intra-individual variance2021-2022Intra-individual variance in the number of cumulus-oocyte-complexes retrieved between first and second cycle in subgroups on the prospectively collected data and historical controls
SecondarySafety of treatment2021-2022Incidence of adverse events related to treatment and assessed by CTCAE v4.0 of follitropin delta in a real-world setting
SecondaryChange in AMH2021-2022Difference in serum AMH values between 1st and 2nd cycle in subjects undergoing two cycles

Outcomes0

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

None in this release.

Results by group0

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

None in this release.

Participant flow0

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

None in this release.

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 totals0

The totals the trial posted for each group.

None in this release.

Papers18

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
16126753BACKGROUNDPubMed
16891297BACKGROUNDPubMed
16923748BACKGROUNDPubMed
17376819BACKGROUNDPubMed
19007627BACKGROUNDPubMed
19793843BACKGROUNDPubMed
19828144BACKGROUNDPubMed
22473395BACKGROUNDPubMed
22698637BACKGROUNDPubMed
23271957BACKGROUNDPubMed

1 to 10 of 18

See all 18 papers

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 comparisons0

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

None in this release.

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/NCT05173597

GET https://conductscience.org/api/trials/v1/NCT05173597/registered