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USG Doppler in high-risk pregnant females to predict adverse outcomes in their babies.

A Prospective observational study of fetal color Doppler and evaluation of Cerebroplacental Ratio as a predictor of adverse perinatal outcome in high risk pregnancy. - Nil

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/05/067993
Enrollment
60
Registered
2024-05-28
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: O099- Supervision of high risk pregnancy, unspecified Health Condition 2: O093- Supervision of pregnancy with insufficient antenatal care Health Condition 3: O092- Supervision of pregnancy with other poor reproductive or obstetric history

Interventions

Control Intervention1: NA: NA

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Pregnant females with Anaemia DM (without any episode of hypoglycaemia) HTN (without any episode of hypertensive urgency/ emergency) Hypothyroidism (without any episode of hypothyroidism coma) PIH and its spectrum. Connective tissue disorders. Rh Negative Pregnancy. Females with Heart diseases

Exclusion criteria

Exclusion criteria: Pregnancies complicated by foetal anomaly or Aneuploidy. Intra-uterine foetal demise. Women undergoing caesarean section for indication other than intrapartum fetal compromise (IFC). Diabetic females with episode/s of hypoglycaemia during pregnancy. Hypertensive females with episodes of hypertensive urgency or emergency during pregnancy. Females with hypothyroidism having any episode of hypothyroidism coma during pregnancy.

Design outcomes

Primary

MeasureTime frame
To calculate Pulsatility Index, Resistive Index and Systolic/ Diastolic Ratio of Umbilical Artery, Middle Cerebral Artery and Uterine Arteries. To calculate the Cerebroplacental Ratio.Timepoint: 28 week to 41 week 6 days of Pregnancy.

Secondary

MeasureTime frame
To predict Adverse perinatal outcome in fetus. To decrease fetal mortality. To aid in deciding further preventive steps in pregnancyTimepoint: 28 week to 41 week 6 days of Pregnancy.

Countries

India

Contacts

Public ContactDr Anjali Mishra

Radiology department, Sir Takhtasinhji General Hospital, Bhavnagar

drmehandi@rediffmail.com9026277600

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026