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HIVNCT07425067

Upper Gastrointestinal Endoscopy in HIV-infected Individuals

An observational study of HIV, run by Centre Hospitalier Universitaire Saint Pierre at 1 site in Belgium.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The aim of this registry is to collect prospectively demographic characteristics and upper gastrointestinal endoscopy diagnoses over a long-term period, in people living with HIV, undergoing upper gastrointestinal endoscopy Read more about this study

Who is it for?
Ages 18 to 99 years
Conditions the study is for
HIV
What is being tested?
Gastroscopy
How many people
2,500 participants
Where
1 siteBelgium
Study dates
1 Jan 2004to 1 Jan 2027
How long will I take part?
1 Day
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 99 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Ppeople living with HIV, undergoing upper gastrointestinal endoscopy

Inclusion criteria: adults aged 18 years or older; first upper gastrointestinal endoscopy; written informed consent.

Exclusion criteria: inability to provide informed consent or refusal.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Belgium1 site, 1 recruiting
  • CHU Saint Pierre

    Brussels, 1000

    Marcel Nkuize, PhD, +32 2 5354658, marcel.nkuize@stpierre-bru.be

    Marcel Nkuize, PhD

    Recruiting

Other trials in Belgium

About this study

The aim of this registry is to collect prospectively demographic characteristics and upper gastrointestinal endoscopy diagnoses over a long-term period, in people living with HIV, undergoing upper gastrointestinal endoscopy

Conditions
HIV
Being tested
Gastroscopy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • GastroscopyDiagnostic test

Study groups in NCT07425067
Study groupRoleWhat they receive
Upper endoscopy in HIV infected patientsNot described
Receives: Diagnostic Test: Gastroscopy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Outcome: demographic, clinical characteristics; endoscopy findings; and pathology diagnoses

    Measured: 2026

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Feb 2026
  2. Study start1 Jan 2004
  3. Primary completion1 Jan 2027 (estimated)
  4. Study completion1 Jan 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Other
Enrolment
2,500 participants (estimated)
Target duration
1 Day
IDs, dates and publications
ClinicalTrials.gov ID
NCT07425067
Sponsor's protocol ID
B07620073105
Status last verified
Oct 2025
First submitted
13 Feb 2026
Last updated
20 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of HIV, run by Centre Hospitalier Universitaire Saint Pierre at 1 site in Belgium.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 20 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Belgium. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Marcel Nkuize, PhD (+32 25354658, marcel.nkuize@stpierre-bru.be), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Outcome: demographic, clinical characteristics; endoscopy findings; and pathology diagnoses (time frame: 2026). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Feb 2026.

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