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Ambulatory blood pressure monitoring vs home based blood pressure monitoring in high risk pregnant females

Role of ambulatory blood pressure monitoring in diagnosis of hypertensive disorders during pregnancy in high risk antenatal females : a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/042956
Enrollment
104
Registered
2022-06-01
Start date
Unknown
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

None listed

Interventions

Intervention1: Ambulatory Blood pressure monitoring: Ambulatory blood pressure monitor is applied to non-dominant arm of the patient for 24 Hours while patient performs their usual activities. Measure

Sponsors

AIIMS Jodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All antenatal females at their first visit in OPD, will be screened for the risk of developing HDP in the present pregnancy. They will be categorized into high risk or low risk for HDP on the basis of presence of one of the following criteria: Presence of any one of the following severe factors: 1. Hypertensive disease during a previous pregnancy 2. Chronic kidney disease 3. Autoimmune disease such as systemic lupus erythematosus or antiphospholipid syndrome 4. Type 1 or type 2 diabetes OR Presence of more than 1 of the following moderate factors: 1. first pregnancy 2. age 35 years or older 3. pregnancy interval of more than 10 years 4. body mass index (BMI) of 30 kg/m2 or more (pre-pregnancy weight or weight at first visit) 5. family history of pre-eclampsia 6. multi-fetal pregnancy

Exclusion criteria

Exclusion criteria: EXCLUSION CRITERIA: 1. High risk antenatal females with office BP > or equal to 150/100 mmHg at first antenatal visit 2. Chronic hypertension 3. Already diagnosed HDP 4. Antenatal females not willing to participate in the study

Design outcomes

Primary

MeasureTime frame
To compare the overall incidence of Hypertensive disorders of pregnancy in high risk antenatal females diagnosed with ABPM v/s those diagnosed with HBPM.Timepoint: 18 months for recruitment

Secondary

MeasureTime frame
To compare mean number of weeks of developing hypertensive disorder of pregnancy after enrollment in studyTimepoint: 18 months;To compare the adverse perinatal outcome in HDP diagnosed females in both the groups.Timepoint: 18 months for recruitment

Countries

India

Contacts

Public ContactDr Priyanka Kathuria

AIIMS Jodhpur

dr.priyankathuria@gmail.com7014982778

Outcome results

None listed

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