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OpenTrials
Completed

NCT Number: NCT03171688

Risk Factors for Nausea and Vomiting After Cesarean

Investigators will observe the incidence of post-cesarean nausea or vomiting and try to associate it with some risk factors.

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Key information

Age range

18 year–100 year

Sex eligibility

Female

Study type

Observational

Primary location

University Hospital of Brasilia University

Brasília, Federal District, 7000000, Brazil

About this study

A single prospective cohort of women submitted to cesarean section who received spinal anesthesia will be assessed for the proposed risk factors and the incidence of nausea or vomiting will be observed during the first 48 hours.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Cesarean section indicated
  • Spinal anesthesia indicated

Exclusion criteria

  • Cesarean section did not occur
  • Spinal anesthesia was not provided
  • Another spinal technique was added to spinal

Treatment and study plan

Primary outcomes

  1. Postoperative Nausea or vomiting

    Time frame: 48 hours.

    The occurrence of postoperative nausea or vomiting, reported by the patient or witnessed by a healthcare provider during the first 48 hours after the cesarean. It is a dichotomic (true or false) outcome.

Sponsors and collaborators

Lead sponsor

Brasilia University Hospital

Other

Registry information

Official study title

Risk Factors for Nausea and Vomiting After Cesarean: Observational Prospective Study

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
May 31, 2017
Registry last updated
Jan 2, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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