Early PONV: Registry Insights from Swedish Perioperative Data

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study analyzes data from the Swedish Perioperative Registry (SPOR) from 2016 to 2022 to estimate the risk of early postoperative nausea and vomiting (PONV) at the recovery unit. It compares cohorts defined by procedure type or time period and identifies factors associated with early PONV. Data are extracted yearly from SPOR, with hospitals able to contribute additional PONV data if they record it, facilitating national-level risk description. No experimental intervention is performed; the aim is descriptive risk characterization and identification of potential predictors. The project leverages a large, real-world surgical dataset to inform future prevention efforts.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Procedure under general or regional anaesthesia
* Age \>=18 years at the day of the procedure.

Exclusion Criteria:

* No entry of the PONV-variable in the SPOR-registry

Where it's running

• Västernorrland County Council / Sundsvall Hospital
  Sundsvall, X, Sweden Recruiting

Study contacts

• Principal investigator: Jakob Wallden, MD PhD — Region Västernorrland (Västernorrland County Council)
• Study coordinator: Jakob Wallden, MD PhD
• Email: jakob.wallden@umu.se
• Phone: 0046703644392

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.