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Continuously Iterative Perioperative Holistic Evaluation of Risk and Hypotension Prediction Index (CIPHER-HPI)

U

University Hospital Southampton NHS Foundation Trust

Status

Not yet enrolling

Conditions

Surgery--Complications

Treatments

Device: Hypotension Prediction Index

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT04807036
RHM CRI0405

Details and patient eligibility

About

The investigators would like to explore whether Hypotension Prediction Index during and immediately after surgery can be used to improve the accuracy of scores that predict postoperative problems.

Full description

It is known that some patients have a prolonged and difficult recovery after major surgery, which impacts their long-term health and wellbeing. A major issue is that scores for predicting recovery are typically generated only once in the period before surgery, but subsequent events during and immediately after surgery can also alter the likelihood of a prolonged and difficult recovery.

One such event appears to be low blood pressure (hypotension). Hypotension Prediction Index can be calculated from routine blood pressure measurements, and is an indicator of blood pressure instability. The investigators propose that Hypotension Prediction Index during and immediately after surgery may be used to improve their accuracy of scores that predict postoperative problems.

To explore this, the investigators will collect information about the health and care needs, surgery and postoperative recovery of adult patients' requiring major surgery. This data will be taken from hospital information systems, a bedside monitor, test reports, a questionnaire and National Databases. The investigators will then use statistical models to determine whether Hypotension Prediction Index improves the accuracy of preoperative scores for predicting postoperative problems.

Ultimately, the investigators hope to create a tool for predicting how well a patient will recover based on the information available at any given point in time. Healthcare professionals will be able to use this tool to identify and support the needs of patients who need extra help recovering from major surgery.

Enrollment

150 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients who:

  1. are referred for CPET
  2. are scheduled for elective surgery and expected to have >24 hours postoperative hospital stay
  3. will receive invasive arterial pressure monitoring as part of routine care
  4. are aged 18 or over
  5. have the capacity to give consent to participate

Exclusion criteria

Patients who:

  1. do not proceed to surgery following CPET referral
  2. are aged less than 18 years
  3. do not have capacity to consent
  4. decline to consent

Trial contacts and locations

0

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Central trial contact

Professor M Grocott; James Badger

Data sourced from clinicaltrials.gov

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