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Swallow a robot camera instead of a tube? new trial tests less scary anaemia exam

NCT ID NCT07197424

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests a robot-assisted capsule (a pill-sized camera) to examine the stomach and small bowel in people with iron deficiency anaemia whose cause hasn't been found by standard tests. The goal is to see if this less invasive method works as well as traditional upper endoscopy (a tube with a camera). 100 adults will swallow the capsule, and doctors will compare what it finds with previous endoscopy results.

What this could mean

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

Active substance
robot assisted magnetically controlled capsule endoscopy
What this could lead to
If successful, this could offer a less invasive, more comfortable way to examine the upper gut and small bowel for causes of iron deficiency anaemia, potentially replacing standard endoscopy.
What could go wrong
This is an early-stage study with only 100 participants, so results may not apply to everyone. The capsule may miss some findings that standard endoscopy would catch.

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

About 100 people

The number the study aims to enrol. It can still change while the study runs.

Started

May 2026

Expected to finish

Mar 2027

An estimate. End dates often move.

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: * Adult patients aged 18 and above * Confirmed diagnosis of iron deficiency anaemia (either recent onset or recurrent) * No significant cause for iron deficiency anaemia previously identified on upper GI endoscopy, colonoscopy or CT colonography * Patients who would either have proceeded directly to small bowel capsule endoscopy (SBCE) or who would have had an initial 'watch and wait' period prior to undergoing SBCE Exclusion Criteria: * Known or suspected gastrointestinal obstruction, strictures or fistulae * Previous abdominal surgery * Dysphagia * Patients with a pacemaker, defibrillator or other implanted electronic device * In vivo retention with medical metal fittings - shunts, plates, stents or clips * A history of metal fragments in the eyes or elsewhere in the body * Confirmed or possible pregnancy * Patients who are not deemed to have capacity according to the Adults with Incapacity Act * Patients who are currently part of another research study

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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.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Leith Community Treatment Centre

    RECRUITING

    Edinburgh, United Kingdom

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