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New blood marker could speed up diagnosis of deadly gut condition

NCT ID NCT03671928

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looked at whether a substance called glicentin in the blood can help diagnose intestinal ischemia, a condition where blood flow to the gut is blocked. Researchers measured glicentin levels in 54 people with suspected ischemia and compared them to a control group. The goal is to find a better, faster way to diagnose this serious condition, which currently has poor diagnostic tools.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could lead to a new blood test to diagnose intestinal ischemia faster and more accurately, potentially saving lives.
What could go wrong
This is a small, early-stage study with only 54 participants. The results may not be strong enough to create a reliable test, and the findings need confirmation in larger trials.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

54 people

The number who actually took part.

Started

Feb 2020

Finished

Mar 2023

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * For patients with intestinal ischemia * The combination of abdominal pain, altered general condition with abdominal defence and venous or arterial hyperlactatemia will be signs suggestive of a diagnosis of digestive ischemia. * Patients suspected of digestive ischemia with the following comorbidities may be included as clinical suspicion and excluded post-operatively: emboligenic heart disease, arteriopathy, aortic and/or digestive atheromatosis. * Patients with suspected digestive ischemia and functional scanning ileus. * Patients with intestinal ischemia proven by CT scan with contrast injection: arterial abnormality such as dissection of an artery for digestive use, thrombosis or embolism of an artery for digestive use; intestinal or colonic thickening suggestive of reversible ischemic suffering of the digestive tract; parietal pneumatosis; gastrointestinal parietal enhancement abnormality (hypo-density ranges or total absence of enhancement). The following pathologies will be taken into account: mesenteric ischemia by embolism or thrombosis. * Age over 18 years old * Able to understand the study * Affiliation to a social security system * Signing of an informed consent * Accept participation in the study (collection of a Non-Opposition) For the control group * Age over 18 years old * Able to understand the study * Affiliation to a social security system * Signing of an informed consent * No personal history of colorectal cancer and obesity * Admission to the Emergency Department of the University Hospital of Nice for abdominal pain with EVA \> 3/10 of non-intestinal origin: nephritic colic, hepatobiliary pathology, gynaecological disease, etc. * Abdominal CT excluding digestive tract pathology * Accept participation in the study Exclusion Criteria: * History of bariatric or digestive surgery (stomach, small intestine, colon or rectum) * History of chronic inflammatory bowel disease * Obese patients (BMI\> 30kg/m2) * History of type 1 diabetes or insulin treatment

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • University Nice Hospital

    Nice, 06000, France