NCT03459989

Brief Summary

We are going to do 2d ultrasound to compare between hadlock's formula and thigh soft tissue formula in expecting the after birth fetal weight and to find which of these formulas to be more accurate

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2017

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 15, 2017

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

March 4, 2018

Completed
5 days until next milestone

First Posted

Study publicly available on registry

March 9, 2018

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2018

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 30, 2018

Completed
Last Updated

August 28, 2018

Status Verified

August 1, 2018

Enrollment Period

1.3 years

First QC Date

March 4, 2018

Last Update Submit

August 26, 2018

Conditions

Estimation of Fetal Weight

Keywords

hadlockthigh soft tissue

Outcome Measures

Primary Outcomes (1)

  • Fetal weight

    hadlock's 4th formula and thigh soft tissue formula

    38 weeks to 40 weeks of gestation

Study Arms (1)

pregnant women

we will measure expected fetal weight by ultrasound by hadlock's formula and thigh soft tissue for each pregnant woman

Diagnostic Test: Ultrasound

Interventions

UltrasoundDIAGNOSTIC_TEST

Samsung H60 Ultrasound

pregnant women

Eligibility Criteria

Age19 Years - 40 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailspregnant women between 38 weeks and 40 weeks
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

The study population comprises 200 pregnant women at 38 to 40 week of gestation attending outpatient clinic and emergency Ain Shams University Maternity Hospital, Obstetrics and Gynaecology Department, Faculty of medicine.

You may qualify if:

  • Gestational age 38 - 40 wks
  • Singleton uncomplicated pregnancies
  • Normal amniotic fluid volume

You may not qualify if:

  • Women with one of the following conditions:
  • Fetuses with congenital anomalies,
  • The biometric measurements of those, which were unable to ascertain due to reasons like deeply engaged head, very thick abdominal wall etc.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ain Shams Universitiy

Cairo, Egypt

RECRUITING

MeSH Terms

Interventions

Ultrasonography

Intervention Hierarchy (Ancestors)

Diagnostic ImagingDiagnostic Techniques and ProceduresDiagnosis

Study Officials

  • Adel SH Salah El-Din, Professor

    Ain Shams University

    STUDY CHAIR

Central Study Contacts

Mohamed Elsenity, Lecturer

CONTACT

+201226573332m.elsenity@yahoo.com

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

March 4, 2018

First Posted

March 9, 2018

Study Start

May 15, 2017

Primary Completion

September 1, 2018

Study Completion

October 30, 2018

Last Updated

August 28, 2018

Record last verified: 2018-08

Locations

EG(1)