Anesthetic and Obstetric Outcomes in Morbidly Obese Pregnancy and Cesarean Delivery

NCT ID: NCT03590951

Last Updated: 2018-07-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

771 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-05-03

Study Completion Date

2018-02-13

Brief Summary

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Given that morbid obesity has been strongly associated with obstetric, neonatal and anesthetic complications, and that scarce reports have evaluated anesthetic and obstetric outcomes after cesarean delivery in morbidly obese patients; This study retrospectively analyzed anesthetic, obstetric and neonatal outcomes in morbidly obese pregnant patients who underwent cesarean delivery at Augusta University Medical Center, during a 2-year period (2015-2016).

Detailed Description

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This study compared non-obese, obese and morbidly obese patients with respect to maternal, perinatal and anesthetic outcomes. Obstetric aspects included emergent procedure, estimated blood loss, obstetric complications, maternal disposition, length of stay and in-hospital mortality. Neonatal aspects included Apgar scores. Anesthetic aspects included anesthetic technique, intraoperative hemodynamic instability, failed regional anesthesia and anesthetic complications.

Conditions

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Morbid Obesity Cesarean Section Complications Pregnancy Related

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Interventions

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Retrospective chart review

A retrospective chart review was conducted to evaluate the effect of body mass index on obstetric, anesthetic and neonatal complications in patients who underwent cesarean section at our institution

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Pregnant patients who underwent cesarean section at Augusta University Medical Center.
* Patients older than 18 years.

Exclusion Criteria

* Gestational age \<37 weeks.
* Patients with chronic pain conditions
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Augusta University

OTHER

Sponsor Role lead

Responsible Party

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Efrain Riveros Perez, MD

Assistant Professor Department of Anesthesiology and Perioperative Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Efrain Riveros Perez, MD

Role: PRINCIPAL_INVESTIGATOR

Medical College of Georgia. Augusta University

Locations

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Augusta University

Augusta, Georgia, United States

Site Status

Countries

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United States

Other Identifiers

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1053583

Identifier Type: -

Identifier Source: org_study_id

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