AzTrials
AzTrials

Gastroesophageal RefluxNCT03524781

Treatment of Newly Diagnosed Gastroesophageal Reflux Disease in a National Population-based Cohort

An observational study of Gastroesophageal Reflux, run by University of Southern Denmark at 1 site in Denmark.

Completed

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

Official record
Search all trials

Trial summary

This study evaluates the treatment of newly diagnosed gastro-esophageal reflux disease in a Danish national cohort, comparing medical and surgical treatment. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Gastroesophageal Reflux
How many people
36,292 participants
Where
1 siteDenmark
Study dates
2 May 2018to 1 Aug 2020
How long will I take part?
2 Years
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patient selection will be done through the Danish National Patient Register. Included will be the period 2000-2015 for a total of 15 years of follow-up. All adult Danish patients diagnosed with GERD and GERD-related diagnosis will be identified (ICD-10 DK21.0-21.9B \& DK20.9B). Patients with GERD-diagnosis within previous two years or with concomitant diagnosis requiring independent anti-secretory treatment will be excluded (DK25.0-9, DK26.0-9, DK27.0-9, DK22.7 \& DE16.4B). To validate GERD-diagnosis, upper endoscopy must have been performed no more than three months before time of diagnosis.

Who may be able to join

  • Danish adult patient with GERD-diagnosis verified by upper endoscopy 1997-2014

Who cannot join

  • Any diagnosis of cancer in the gastrointestinal tract during follow-up
  • Patients with GERD-diagnosis within previous four years or with concomitant diagnosis requiring independent anti-secretory treatment will be excluded (DK25.0-9, DK26.0-9, DK27.0-9, DK22.7 \& DE16.4B).

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Department of Surgery, Kolding Hospital

    Kolding

Other trials in Denmark

About this study

This study evaluates the treatment of newly diagnosed gastro-esophageal reflux disease in a Danish national cohort, comparing medical and surgical treatment.

Read the detailed description

Aim: To compare rate of surgery with medical treatment in patients with newly diagnosed gastro-esophageal reflux disease in a nationwide population based cohort over 15 years.

Background: Between 1990 and 1997, frequency of anti-reflux surgery in USA rose from 4,4 per 100.000 inhabitants to 12 per 100.000 inhabitants. In the same period a trans-abdominal laparoscopic approach increased to 64% of cases and mortality as well as morbidity decreased. The operation rate peaked around 2000 with an increase of 260% to approximately 16.7 operations per 100.000 inhabitants. Complications fell to its lowest point around 2000 as well.

Hereafter, the frequency of anti-reflux surgery dropped by 40% between 2000 and 2006. Complications in the form of morbidity and mortality rates steadily rose again, but the patients having performed surgery were now older and have longer hospital stays and more comorbidity. A slight rise in frequency of anti-reflux surgery to 6,1 per 100.000 inhabitants was registered in 2010 and at this time length of stay, morbidity and mortality rates have decreased, probably illustrating an increased experience. Interesting to note is, that in the American data, use of laparoscopic approach does tend to plateau at 70-80%.

It is unknown whether anti-reflux surgery in Denmark has followed the same trend. There are important differences in the setup of surgical service that may affect the results, as open anti-reflux surgery never gained much popularity in Denmark. Also, significantly fewer centers offer the procedure. In a study of re-operative anti-reflux surgery based on data from 1997-2005, a primary anti-reflux surgery rate of 5.2 per 100.000 inhabitants was reported. However, we do not know how this rate has developed or was preceded.

Hypothesis: From 2000-2015 there has been an increase in diagnosis of GERD and in the use of anti-secretory drugs, but a decrease in the utilization of anti-reflux surgery.

Methods and materials: Patient selection will be done through the Danish National Patient Registers. Included will be the period 2000-2015 for a total of 15 years of follow-up.

All adult Danish patients diagnosed with GERD and GERD-related diagnosis will be identified (ICD-10 DK21.0-21.9B \& DK20.9B) using The National Patient Registry.To validate GERD-diagnosis, upper endoscopy must have been performed no more than three months before time of diagnosis.

Patients with GERD-diagnosis within previous four years or with concomitant diagnosis requiring independent anti-secretory treatment will be excluded (DK25.0-9, DK26.0-9, DK27.0-9, DK22.7 \& DE16.4B). Patients diagnosed with cancer of the gastrointestinal tract (DC15-26) will also be excluded.

Using the Danish National Prescription Register, use of H2-antagonists (A02BA), proton pump inhibitors (A02BC), prostaglandins A02BB and bismuth, alginate and sucralfate (A02BX) will be identified in daily doses within two years of GERD-diagnosis. Anti-reflux surgery within the same period will be identified from The National Patient Registry using the procedure codes (NOMESCO: KJBC00, KJBC01, KJBC02, KJBW96, KJBW97).

From The National Patient Registry, age, sex and Charlson Comorbidity Index will be retrieved. Mortality during follow-up will be retrieved from The Civil Registration System.

Keywords
Anti-reflux surgery, Proton-pump inhibitors, Upper endoscopy
Medical subject headings
Gastroesophageal Reflux

What is being measured

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

  1. Treatment of GERD

    Medical treatment, surgical treatment or no treatment

    Measured: 2 years after diagnosis

Timeline

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

  1. First posted15 May 2018
  2. Study start2 May 2018
  3. Primary completion1 Jan 2019
  4. Study completion1 Aug 2020

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
36,292 participants (actual)
Target duration
2 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT03524781
Sponsor's protocol ID
JSJ_OP445
Status last verified
Aug 2020
First submitted
2 May 2018
Last updated
4 Aug 2020
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual patient data are by Danish law no allowed to be shared without specific authorization prior to study initiation.

Questions about this trial

What is this clinical trial studying?

An observational study of Gastroesophageal Reflux, run by University of Southern Denmark at 1 site in Denmark.

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 4 Aug 2020. 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 Denmark. 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?

Treatment of GERD (time frame: 2 years after diagnosis). 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 4 Aug 2020.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in