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Non-invasive Haemodynamic Monitoring to Predict Spinal Hypotension During Caesarian Section

H

Hospital Nord

Status

Completed

Conditions

Hypotension
Spinal Anesthetics Causing Adverse Effects in Therapeutic Use
Pregnancy Related

Treatments

Device: Clearsight monitoring

Study type

Observational

Funder types

Other

Identifiers

NCT04608227
Darnord-2020

Details and patient eligibility

About

Spinal anaesthesia for elective caesarean section is associated with maternal hypotension, secondary to alteration of sympathetic tone and hypovolemia, in up to 70% of cases.

Our objective, in this prospective single-centre observational study, was to assess the ability of change in systolic ejection volume after 45° passive leg raising to predict hypotension after spinal anaesthesia. Systolic ejection volum was monitored with non-invasive Clearsight Device just before elective caesarean section in third trimester pregnant women.

Enrollment

40 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • third trimester pregnant women undergoing elective ceasarean section under spinal anesthesia

Exclusion criteria

  • emergent ceasarean section
  • eclampsia or pre-eclampsia
  • undergoing anti-hypertensive treatment
  • arythmia

Trial design

40 participants in 1 patient group

Third trimester pregnant women undergoing ceasarean section
Treatment:
Device: Clearsight monitoring

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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