Not yet recruiting NCT07494669

Proteomics and Physiological Parameters Predicting Complications After Colorectal Cancer Surgery

— Observational Observation Postoperative

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: The protocol lists: Risk stratification with proteomics and data from wearables and CGMs.
Who it may be relevant to: Registry conditions: Observation, Postoperative. Basic parameters: from 18 years · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: Center list to be confirmed — check the primary protocol.
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Towards Precision Perioperative Medicine: Multimodal Prediction of Surgical Complications Using Proteomics and Physiological Monitoring

Overview

Study combines physiological data from wearables, continuous glucose montiors and proteomics to better assess risk of complications after colorectal surgery

Interventions

Diagnostic test Risk stratification with proteomics and data from wearables and CGMs
Risk Stratification

Primary outcome measures

Complications (Clavien-Dindo >0) [Time frame: 30 days postoperatively]

Secondary outcome measures (1)

Serious complications [Time frame: 30 days postoperatively]

Eligibility criteria

Inclusion criteria

Scheduled for elective colorectal cancer surgery

Exclusion criteria

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model: Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07494669 · ProComp

Primary sources (government registries)

ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗