MedTrace Logo

Blind Measurement in Fetal Weight Estimation

NCT06687239 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2024-11-13

No results posted yet for this study

Summary

Woman who are expected to give birth in the next 72 hours will be allocated randomly to a study group of blinded measurements for estimated fetal weight and a control group of non-blinded measurements. Accuracy of estimations will be compared between the groups.

Conditions

  • Pregnancy

Interventions

DIAGNOSTIC_TEST

Blinded estimation of fetal weight

Blinded ultrasound-based estimation of fetal weight

DIAGNOSTIC_TEST

Non blinded estimation of fetal weight

Non-blinded ultrasound-based estimation of fetal weight

Sponsors & Collaborators

  • Eran Brazilay, MD PhD

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-12-31
Primary Completion
2025-12-31
Completion
2025-12-31

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06687239 on ClinicalTrials.gov