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Effect of Increased BMI on Efficacy of Labor Analgesia

M

Mariah Arif

Status

Completed

Conditions

Neuraxial Analgesia
Labor Analgesia

Treatments

Procedure: Neuraxial Analgesia
Procedure: Neuraxial analgesia

Study type

Observational

Funder types

Other

Identifiers

NCT07367347
MRC-01-24-875

Details and patient eligibility

About

This study seeks to identify the most effective neuraxial technique for labor analgesia in Class III parturient

Full description

This retrospective cohort study collected data on eligible participants from the electronic medical records.

Enrollment

9,000 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age > or equal to 18 years
  • BMI ≥ 40 kg/m²
  • Gestational age ≥ 28 weeks

Exclusion criteria

  • Age < 18 years
  • BMI < 40 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

9,000 participants in 1 patient group

Class III obese parturient
Description:
Class III obese parturient receiving neuraxial analgesia
Treatment:
Procedure: Neuraxial analgesia

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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