ClinicalTrials.gg
Not yet recruitingNCT06620068VEGF PPUpdated Oct 1, 2024

Causal Relationship Between Plasma VEGF Family Proteins and Placenta Previa: A Two-Sample Mendelian Randomization Study

An observational study in Placenta Previa, sponsored by Guangzhou Institute of Respiratory Disease. Not yet recruiting. Per ClinicalTrials.gov, last updated 2024-10-01.

Sponsored by Guangzhou Institute of Respiratory Disease · Observational

From the registry’s dates

  • Primary completion was expected by Nov 2024, 2 years ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Other
Time perspective
Retrospective
Enrollment
207,473
Sex
All
01

Study summary

This study aims to investigate the causal relationship between plasma vascular endothelial growth factor (VEGF) family proteins and placenta previa using a two-sample Mendelian randomization (MR) approach. Genome-wide association study (GWAS) data will be analyzed to assess the correlation and potential causality between VEGF protein levels and the occurrence of placenta previa.

Read the detailed description

Placenta previa is a serious complication during pregnancy, leading to significant risks for both the mother and the fetus. This study utilizes Mendelian randomization (MR) to explore the potential causal link between plasma levels of VEGF family proteins (including VEGFA, VEGFB, VEGFC, VEGFD, and PLGF) and the risk of placenta previa. By using genome-wide association study (GWAS) data from the UK Biobank and FinnGen datasets, the study aims to provide insights into the role of angiogenesis and abnormal placental development. The MR analysis will help minimize confounding factors and provide robust evidence regarding the causal relationship between VEGF proteins and placenta previa.

02

Conditions studied

  • Placenta Previa

Keywords

  • Vascular Endothelial Growth Factor (VEGF)
  • Mendelian Randomization
  • Angiogenesis
  • Pregnancy Complications
  • Placental Development
03

In context

Placenta Previa

80 studies on the registry are indexed under Placenta Previa; 17 are open to participants now.

This study's planned enrollment of 207,473 is above the median of 100 across 32 observational studies indexed under Placenta Previa.

Browse Placenta Previa studies →

Lead sponsor

Guangzhou Institute of Respiratory Disease is the lead sponsor of 99 studies on the registry; 18 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

This study analyzes data from European populations included in genome-wide association studies (GWAS) from UK Biobank and FinnGen, focusing on individuals with available plasma VEGF family protein levels and placenta previa data.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Participants included in genome-wide association studies (GWAS) with available data on plasma VEGF family proteins and placenta previa.

Exclusion criteria

Exclusion Criteria:

  • Participants with incomplete or missing data on plasma VEGF levels or placenta previa.
05

Study design

Observational model
Other
Time perspective
Retrospective
Enrollment
207,473 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna
06

What researchers measure

Primary outcomes

  1. Causal relationship between plasma VEGFA levels and the risk of placenta previa

    This outcome measures the association between plasma VEGFA levels (measured in picograms per milliliter) and the occurrence of placenta previa, using Mendelian Randomization (MR) analysis to assess causality.

    Time frame: Data analysis and outcome assessment will be completed by December 2024

Secondary outcomes

  1. Causal relationship between plasma VEGFB levels and the risk of placenta previa

    This outcome measures the association between plasma VEGFB levels (measured in picograms per milliliter) and the occurrence of placenta previa, using Mendelian Randomization (MR) analysis to assess causality.

    Time frame: Data analysis and outcome assessment will be completed by December 2024

  2. Causal relationship between plasma VEGFC levels and the risk of placenta previa

    This outcome measures the association between plasma VEGFC levels (measured in picograms per milliliter) and the occurrence of placenta previa, using Mendelian Randomization (MR) analysis to assess causality.

    Time frame: Data analysis and outcome assessment will be completed by December 2024

  3. Causal relationship between plasma PLGF levels and the risk of placenta previa

    This outcome measures the association between plasma PLGF levels (measured in picograms per milliliter) and the occurrence of placenta previa, using Mendelian Randomization (MR) analysis to assess causality.

    Time frame: Data analysis and outcome assessment will be completed by December 2024

07

Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Sep 2024; primary completion for Nov 2024, 1 month later.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 24, 2024
First posted
Oct 1, 2024
StartEst.
Sep 25, 2024
Primary completionEst.
Nov 1, 2024
CompletionEst.
Dec 1, 2024
Last update
Oct 1, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Oct 1, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06620068
Lead sponsor
Guangzhou Institute of Respiratory Disease
Collaborators
The Second People's Hospital of Foshan, First People's Hospital of Foshan, Maternal and Child Health Hospital of Foshan
Responsible party
Zhibin Xu (Professor, Guangzhou Institute of Respiratory Disease) — Principal investigator
First posted
Oct 1, 2024
Start date
Sep 25, 2024 (estimated)
Primary completion
Nov 1, 2024 (estimated)
Completion
Dec 1, 2024 (estimated)
Last update
Oct 1, 2024

Study contacts

Zhibin Xu
Contact
unignorable_xuzhibin@outlook.com
+8615816832640

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion