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Repeatedly Recurring EsophagitisNCT01562639

Nexium Capsules RE Maintenance Specific Clinical Experience Investigation

An observational study of Repeatedly Recurring Esophagitis and Relapsing Reflux Esophagitis, run by AstraZeneca at 46 sites in Japan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to collect following data in patients given Nexium capsule (Nexium) in usual post-marketing use as the maintenance therapy for repeatedly recurring/relapsing reflux oesophagitis. Read more about this study

Who is it for?
Any age
How many people
647 participants
Where
46 sitesJapan
Study dates
Apr 2012to Jul 2014
Phase
Observational
Are there results?
None posted in the registry

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 Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Patients with repeatedly recurring/relapsing reflux oesophagitis who will be given Nexium for the first time as a maintenance therapy. (Patients who had been given Nexium for the initial treatment for reflux oesophagitis can be enrolled to this investigation).

Who may be able to join

  • Patients with repeatedly recurring/relapsing reflux oesophagitis who will be given Nexium for the first time as a maintenance therapy.

Who cannot join

  • Patients having reflux oesophagitis when Nexium is started (Grade A, Grade B, Grade C or Grade D of Los Angeles Classification (Hoshihara's modification) on endoscopy)
  • Patients having previous history of maintenance therapy for repeatedly recurring/ relapsing reflux oesophagitis

Trial locations and contacts

46 sites in 1 country.

46 sites in 1 country

Japan46 sites
  • Research Site

    Aichi

  • Research Site

    Akita

  • Research Site

    Aomori

  • Research Site

    Chiba

  • Research Site

    Ehime

  • Research Site

    Fukui

  • Research Site

    Fukuoka

  • Research Site

    Fukushima

  • Research Site

    Gifu

  • Research Site

    Gunma

  • Research Site

    Hiroshima

  • Research Site

    Hokkaido

  • Research Site

    Hyōgo

  • Research Site

    Ibaraki

  • Research Site

    Ishikawa

  • Research Site

    Kagawa

  • Research Site

    Kagoshima

  • Research Site

    Kanagawa

  • Research Site

    Kochi

  • Research Site

    Kumamoto

  • Research Site

    Kyoto

  • Research Site

    Mie

  • Research Site

    Miyagi

  • Research Site

    Miyazaki

  • Research Site

    Nagano

  • Research Site

    Nara

  • Research Site

    Niigata

  • Research Site

    Numakunai

  • Research Site

    Ōita

  • Research Site

    Okayama

  • Research Site

    Okinawa

  • Research Site

    Osaka

  • Research Site

    Saga

  • Research Site

    Saitama

  • Research Site

    Shiga

  • Research Site

    Shimane

  • Research Site

    Shizuoka

  • Research Site

    Tochigi

  • Research Site

    Tokushima

  • Research Site

    Tokyo

  • Research Site

    Tottori

  • Research Site

    Toyama

  • Research Site

    Wakayama

  • Research Site

    Yamagata

  • Research Site

    Yamaguchi

  • Research Site

    Yamanashi

Other trials in Japan

About this study

Official title: Nexium Capsules Specific Clinical Experience Investigation for Maintenance Therapy for Repeatedly Recurring/Relapsing Reflux Oesophagitis

The purpose of this study is to collect following data in patients given Nexium capsule (Nexium) in usual post-marketing use as the maintenance therapy for repeatedly recurring/relapsing reflux oesophagitis.

Read the detailed description

Nexium capsules Specific Clinical Experience Investigation for Maintenance Therapy for Repeatedly Recurring/Relapsing Reflux Oesophagitis

Keywords
maintenance therapy,, repeatedly recurring,, relapsing reflux oesophagitis,, Nexium

What participants receive

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

Study groups in NCT01562639
Study groupRoleWhat they receive
NexiumNot described

What is being measured

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

  1. Number of Adverse Drug Reactions

    Adverse event incidence

    Measured: 6 Month

Secondary outcomes (1)
  1. Non-recurrence rate of reflux oesophagitis

    Measured: 6 Month

Timeline

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

  1. First posted26 Mar 2012 (estimated)
  2. Study startApr 2012
  3. Primary completionJul 2014
  4. Study completionJul 2014

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
Cohort
Time perspective
Prospective
Enrolment
647 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01562639
Sponsor's protocol ID
D961HC00013
Status last verified
Oct 2014
First submitted
22 Mar 2012
Last updated
31 Oct 2014
Results posted
No

Questions about this trial

What is this clinical trial studying?

An observational study of Repeatedly Recurring Esophagitis and Relapsing Reflux Esophagitis, run by AstraZeneca at 46 sites in Japan.

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

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. 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: finished, as of the sponsor's last update on 31 Oct 2014. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 46 sites in Japan. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of Adverse Drug Reactions (time frame: 6 Month). 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 31 Oct 2014.

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