Clinical trial Recruiting at 1 site Observational Ages 18 and up

Does fasting time affect post-induction low blood pressure after anesthesia?

Official title: Evaluation of the Relation Between Patient Fasting Time and the Occurrence of PIH (Post Induction Hypotension) - Prospective Trial

Run by University Hospital Ostrava · NCT07785635 · Data updated 2026-11-12

This observational study tests whether how long a patient fasts before anesthesia changes the chance of post-induction hypotension in adults undergoing planned procedures.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorUniversity Hospital Ostrava
Academic / other
Locations1 site (Ostrava, Moravian-Silesian Region)
StatusRecruiting
StartedMay 1, 2025
Main results expectedSeptember 2026
Study endsSeptember 2026
Registry record updatedAugust 25, 2026
Trial IDNCT07785635 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) scheduled for planned surgical or diagnostic procedures with general anesthesia and intubation.

Probably not a fit

Patients with factors unrelated to fasting time or with PIH due to other causes may not see a benefit.

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

What this trial studies

In this single-center prospective study, researchers examine the relationship between preoperative fasting duration and the occurrence of post-induction hypotension after general anesthesia. The study considers multiple factors contributing to blood pressure drops, including anesthetic effects, ventilation, and relative fluid status due to fasting. Adults undergoing planned surgery or diagnostic procedures with intubation under general anesthesia are observed to assess associations between fasting length and PIH incidence and severity. No interventions are described beyond observation.

Why it matters

Potential benefit: If fasting duration is linked to PIH, clinicians may optimize preoperative fasting guidance to reduce hypotension risk.

How similar studies have gone: Prior knowledge supports that fluid status and vasoplegia contribute to PIH; this study explores a specific, modifiable factor (fasting time) and its impact.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age ≥ 18 years
* Patients undergoing planned surgical or diagnostic procedure
* Intubation under general anaesthesia

Exclusion Criteria:

* Pregnancy
* Disagreement with participation in the study
* Bowel preparation

Where it's running

  • University Hospital Ostrava
    Ostrava, Moravian-Silesian Region, Czechia
    Recruiting

Study contacts

  • Principal investigator: Ondřej Jor, MD, PhD, MBA — University Hospital Ostrava
  • Study coordinator: Jiří Hynčica
  • Email: jiri.hyncica@fno.cz
  • Phone: 0042059737

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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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.