A comparative study between two different ultrasonography parameters of amniotic fluid assessment in women with term pregnancy with their foetal outcome

Correlation of single deepest vertical pocket of amniotic fluid and amniotic fluid index at term with foetal outcome - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/10/074971

Enrollment

150

Registered

2024-10-09

Start date

Unknown

Completion date

Unknown

Last updated

2024-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium

Interventions

Intervention1: Single Deepest Vertical Pocket measurement: In the group assigned to SDVP measurement, only the largest diameter of the fluid pocket will be measured. The deepest pocket of amniotic flu

Eligibility

Inclusion criteria

Inclusion criteria: 1. At term pregnant women with gestational age of 37 to 40 weeks with amniotic fluid assessment done in last 7 days 2. Singleton pregnancy with cephalic presentation 3. Confirmed period of gestation by an ultrasound scan performed in first trimester of pregnancy 4. Intact membranes without rupture on admission to labour room 5. Those patients who are willing to get enrolled in the study

Exclusion criteria

Exclusion criteria: 1. Patients with previous Cesarean section. 2. History of gestational hypertension and/or diabetes mellitus, multiple gestation, premature rupture of the membranes, placenta previa or any other placental anomaly, polyhydramnios, bad obstetrical history, antepartum haemorrhage 3. Structural or chromosomal foetal malformation, intrauterine growth restriction, intrauterine foetal death, RH incompatibility

Design outcomes

Primary

Measure	Time frame
Postpartum admission to neonatal intensive care unit Timepoint: Admission will be done at the time of admission. The study will be carried for a period of 2 years.	—

Secondary

Measure	Time frame
1. Apgar score at birth and at 5 minutes 2. Incidence of oligohydramnios 3. Maternal and fetal factors associated with oligohydramnios 4. Maternal and Obstetrics characteristics 5. Reliability and reproducibility of measurement techniques Timepoint: Assessment will be done at the time of admission. The study will be carried for a period of 2 years	—

Countries

India

Contacts

Public ContactShefali Singh

Jawaharlal Nehru Medical College, Sawangi Meghe, Wardha

sandhyapajai@gmail.com9823686669

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026