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OpenTrials
Completed

NCT Number: NCT04889534

Predictive Factors for Postoperative Pain, Nausea and Vomiting in Oncological Patients

1809 patients were evaluated in postoperative period. They were asked about nausea, vomiting, retching and pain in the first postoperative 24 hours

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Angela Maria Sousa

São Paulo, 01403010, Brazil

About this study

Patients were prospectively evaluated , and nausea, vomiting and pain were recorded.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • patients submitted to oncological surgeries

Exclusion criteria

  • refusal to sign the agreement term
  • lack of information in the records

Treatment and study plan

Analgesia

Procedure

Patients will be observed during postoperative period,

Primary outcomes

  1. Intensity of postoperative pain

    Time frame: 24 hours

    pain intensity was measured using descriptive and verbal number scale

Secondary outcomes

  1. side effects from analgesia

    Time frame: 24 hours

    nausea, vomiting, pruritus and hypotension were measured during first 24 postoperative hours

Sponsors and collaborators

Lead sponsor

Instituto do Cancer do Estado de São Paulo

Other

Collaborators

  • Sponsor GmbH

Registry information

Official study title

Evaluation of Predictive Factors for Nausea, Vomiting and Postoperative Acute Pain in Oncological Patients

Acronym: PONV

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
May 17, 2021
Registry last updated
May 17, 2021

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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