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Impact of Increasing BMI on the Success of Neuraxial Blocks in Class III Obese Parturients

M

Mariah Arif

Status

Completed

Conditions

Neuraxial Blocks

Treatments

Procedure: Neuraxial anesthesia

Study type

Observational

Funder types

Other

Identifiers

NCT07367386
MRC-01-24-905

Details and patient eligibility

About

This study seeks to compare the success rates, feto-maternal outcomes, and complications associated with different neuraxial blocks in Class III obese parturient undergoing cesarean section

Full description

This was a retrospective cohort study. The data was obtained from electronic medical records of the eligible participants.

Enrollment

1,917 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age > or equal to 18 years
  • BMI ≥ 45 kg/m²
  • Gestational age ≥ 28 weeks

Exclusion criteria

  • Age < 18 years
  • BMI < 45 kg/m²
  • History of venous thromboembolism or arterial disease (e.g., DVT, PE, angina, MI, or stroke)
  • Severe active lung, cardiovascular, renal, or liver disorders; autoimmune disease; or hemoglobinopathies
  • Hereditary or acquired thrombophilia (e.g., Factor V Leiden mutation or antithrombin deficiency)
  • In utero fetal demise (IUFD)
  • Failed operative vaginal delivery
  • Cesarean for the second twin or multiple pregnancies (triplets or higher)
  • IVF pregnancy
  • Intraoperative bleeding>1500mL
  • Emergency cesarean section (Category I)
  • Presence of large uterine fibroid ≥10 cm

Trial design

1,917 participants in 1 patient group

Class III obese parturient
Description:
Class III obese parturient undergoing cesarean section under neuraxial block
Treatment:
Procedure: Neuraxial anesthesia
Procedure: Neuraxial anesthesia
Procedure: Neuraxial anesthesia

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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