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Relationship between symphysiofundal height and abdominal girth with the occurrence of hypotension in cesarean section under spinal anaesthesia using 0.5% Hyperbaric bupivacaine

Correlation of symphysiofundal height and abdominal girth with the incidence of hypotension in cesarean section under spinal anaesthesia using 0.5% Hyperbaric bupivacaine

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/01/048966
Enrollment
42
Registered
2023-01-12
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

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

Conditions

None listed

Interventions

None listed

Sponsors

Amala Cynthia Empress E
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American society of Anaesthesia grade II Body Weight 50 - 75 Kg Patient undergoing elective cesarean section with singleton pregnancy

Exclusion criteria

Exclusion criteria: Parturients in active labor Placenta previa Oligohydraminos or polyhydraminos Pregnancy induced hypertension/ Gestational diabetes mellitus Significant medical or obstetric morbidity Obstructed labor, abnormal lie/ presentation More than two previous cesarean section Mental incapacity or language barrier precluding to informed consent Patient refusal

Design outcomes

Primary

MeasureTime frame
Among the two parameters (Symphysiofundal height and abdominal girth), symphysiofundal height will have increased incidence of hypotension in cesarean section under spinal anaesthesia using 0.5% Hyperbaric bupivacaineTimepoint: Systolic and diastolic blood pressure, mean arterial blood pressure and level of sensory blockade will be measured at regular intervals—

Secondary

MeasureTime frame
Symphysiofundal height will have increased incidence of hypotension in cesarean section under spinal anaesthesia using 0.5% Hyperbaric bupivacaineTimepoint: Systolic and diastolic blood pressure, mean arterial blood pressure and level of sensory blockade will be measured from beginning of procedure till the end of procedure—

Countries

India

Contacts

Public ContactKrishna Prabu

Sri Venkateshwaraa Medical College Hospital and Research Centre

drkrishnaprabu@gmail.com9943770977

Outcome results

None listed

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