None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Live fetus 2.Term pregnancy (Gestational age of 37-40 weeks) 3.Singleton pregnancy 4.Cephalic presentation 5.Known last menstrual period or ultrasound scan with confirmed expected date of delivery
Exclusion criteria
Exclusion criteria: 1.Multiple gestation 2.Non- cephalic presentation 3.Intrauterine fetal death 4.Presence of coexisting fibroids or adnexal masses 5.Already diagnosed liquor abnormalities 6.known fetal malformation 7.obesity
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of this study is to compare the estimated fetal weight obtained from clinical methods (Johnson’s formula, Insler’s formula, and McDonald’s measurement of symphysio-fundal height) and ultrasound (using Hadlock’s formula) with the actual birth weight of the neonate. This comparison will assess the accuracy and reliability of each method in predicting fetal weight and provide insights into their clinical utility in a tertiary care hospital setting in Central India.Timepoint: The study shall be conducted between 37 to 40 weeks of pregnancy | — |
Secondary
| Measure | Time frame |
|---|---|
| accuracy of fetal weight estimation correlation coefficients factors influencing accuracy clinical utilityTimepoint: the study shall be conducted between 37 to 40 weeks of pregnancy | — |
Countries
India
Contacts
Datta Meghe institute of higher education and research