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Complications After Gastric Bypass OperationNCT01930851

Complications After Bariatric Surgery Based, a Questionnaire Survey

An observational study of Complications After Gastric Bypass Operation, run by University of Aarhus 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
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Trial summary

The number of obese is increasing rapidly. Bariatric surgery is used to a greater and greater extent as treatment of obesity to obtain a greater and more permanent weight loss. The currently most commonly used surgical method is the gastric bypass (RYGB), which so far has proved to be the most effective way to achieve… Read more about this study

Who is it for?
Ages 18 to 70 years
What is being tested?
Gastric bypass operation
Type of treatment
Surgery or procedure
How many people
1,429 participants
Where
1 siteDenmark
Study dates
Feb 2014to Aug 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 18 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Gatric bypass operated patients in the Central Denmark Region

Who may be able to join

  • gastric bypass operation 206-2011
  • Residents i the Central Denmark Region

Who cannot join

  • -

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • department of endocrinology and metabolism, Aarhus University Hospital

    Aarhus, 8000

Other trials in Denmark

About this study

Official title: Prevalence of Medical and Nutritional Complications After Bariatric Surgery (Gastric Bypass) Based on a Questionnaire Survey

The number of obese is increasing rapidly. Bariatric surgery is used to a greater and greater extent as treatment of obesity to obtain a greater and more permanent weight loss. The currently most commonly used surgical method is the gastric bypass (RYGB), which so far has proved to be the most effective way to achieve a greater and more permanent weight loss, reduction and maybe even elimination of many of the obesity-related health complication (diabetes, sleep apnea, pain due to osteoarthrosis etc.).

Bariatric surgery, including RYGB is also associated with medical and nutritional complications. This will be a natural consequence of the fact that the food bypasses virtually the entire ventricle and 100-150 cm of the upper part of the small intestine after a RYGB. Therefore, problems with uptake of for example B12, iron, folate, thiamin, fat-soluble vitamins (Vitamins A, D, E and K) copper, zinc and selenium are expected. In the light of this, it is decided that all RYGB operated patients must take vitamin B12, iron and vitamin D substitution. In spite of this, many develop various nutritional problems after RYGB. In addition to these nutritional complications are complications such as hypoglycaemia and gallstone attacks after RYGB.

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Nevertheless there is no comprehensive inventory of the occurrence of nutritional complications after bariatric surgery neither in Denmark nor in an international context. Thus there is no consensus on an optimal postoperative prevention of complications. An overview of the occurrence of these problems will be important for assessing and determine the indications for bariatric surgery as well as to optimize the prevention of complications.

To enlighten this we will conduct a questionnaire survey of complications such as pain, dumping and hypoglycemia after RYGB. Moreover we will the quality of life after RYGB operation. We will invite 3500 RYGB operated patients the Central Denmark Region who have been operated 2006-2011.

Read the detailed description

Background Prevalence of overweight and obesity is increasing both in Denmark and in most other countries, and as conventional treatment of obesity with lifestyle changes (hypocaloric diet, physical activity and behavior modification) rarely leads to large and sustained weight loss, it is not surprising that bariatric surgery has taken over more and more of the treatment of the most severe cases of obesity. Weight losses are greater than with other treatments, and importantly the relatively large weight loss is permanent.

Positive effects of gastric bypass The currently most commonly used surgical method is the gastric bypass (RYGB), which has proven to be a highly effective method of achieving a great and permanent weight loss with an approximately 30-40% reduction in the weight, which is equivalent to 40-60% reduction of the overweight. Moreover RYGB has shown to provide complete remission of prior type 2 diabetes in up to 80% of cases at short observation time (up to 2 years after surgery) and about 50% remission at longer time follow-up (> 5 years).

Moreover data suggest that after RYGB there is a reduced consumption of antihypertensive drugs in 51 % and of lipid-lowering drugs in 59 %.

Psychiatric complications after gastric bypass There are conflicting results in the literature when examining the consumption of antidepressants. Some studies find a reduced consumption of antidepressants after bariatric surgery within the first two years, others show that consumption is almost unchanged overall and cohort follow-up studies show an increased quality of life.

Nevertheless, there is an increased incidence of suicide after bariatric surgery, which argues against an unambiguous improvement in psychological well-being.

Nutritional complications after gastric bypass Bariatric surgery including RYGB is also connected with some medical and nutritional effects or complications. This is not surprising since RYGB "bypasses" virtually the entire ventricle and 100-150 cm of the upper part of the small intestine, so problems with the inclusion of, for example B12, iron, folate, thiamin, fat-soluble vitamins (Vitamin A, D, E and K) copper, zinc and selenium are expected. Therefore, it is recommended that all RYGB operated patients substitute vitamin B12, iron and vitamin D. Despite this many develop various nutritional problems after RYGB which in the long term can result in irreversible neurological damage, osteoporosis and anemia. Such complications are sparsely registered in Denmark.

The complications are often developed long time after the operation, at a time when the patients are no longer followed in specialized departments which report all complications to the Danish Obesity Register, in the same way as surgical complications are reported. There is no international consensus on postoperative vitamin substitution, which may be due to the previous lack of evidence of nutritional complications. Other classic side effects are early and late dumping, manifested by weakness after a meal or symptoms of moderate degrees of low blood sugar (hypoglycemia). Frequent bowel movements are an expected result of a GYP, but for some patients as much that they are hampered in their daily activities.

Surgical complications after gastric bypass

International studies have shown that mortality of bariatric surgery ranges between 0.24 and 2.77% depending on the operator and the hospital, and perioperative morbidity ranges between 6.92 and 8.85% also depending on the operator and the hospital.

Moreover complications such as abdominal pain of varying degree and the development of gallstones are frequently seen. Moreover complications such as abdominal pain of varying degree and the development of gallstones are frequently seen.

It is still unresolved how extensive a problem these nutritional complications after bariatric surgery in Denmark are, we want to clarify the occurrence of these complications in Denmark. This will provide an overview of the positive as well as the negative impact of bariatric surgery and thus will be decisive to assess and determine the indications for bariatric surgery as well as to optimize the prevention of complications.

In this project will be made a questionnaire survey where all GYP patients in the Central Denmark Region in the period 2006 - 2011 (about 3500 people) will receive an invitation to participate. This part includes thus measurement of self-reported complications that would otherwise not be detected through other registers or records, and measurement of quality of life after GYP

The purpose is as follows:

  1. To describe serious complications (readmissions, reoperations etc) related to complications after GYP
  2. To estimate incidence (prevalence) of the most common nutritional complications after GYP in Denmark
  3. To estimate incidence (prevalence) of neurological complications after GYP in Denmark
  4. To describe the quality of life in patients who have undergone GYP including improvement of disease (e.g. diabetes, sleep apnea, joint pain) after GYP.

Thus, the investigators wish to achieve a better documentation of both the positive effects after GYP (weight loss, remission of diabetes, quality of life, etc.) and the negative health effects (mortality, surgical and nutritional) in order to provide a better founded approach to this form of treatment.

Method From the Central Denmark Region, the investigators will obtain social security numbers of all gastric bypass operated persons in the Central Denmark Region (approximately 3500 patients). From the State Serum Institute will be obtained information on their address from the social security number and they will be invited by letter to participate in the survey. The letter will contain a numbered questionnaire hence the answer is anonymous. The questionnaire will include questions relating to weight loss, surgical complications, possible remission of diabetes, substitution treatment, nutritional complications, hypoglycaemia, quality of life (SF-12), etc.

Data from the questionnaires will be entered electronically and we will conduct statistical analysis based on the patients' responses. Prior to the publication of the questionnaires will be conducted a pilot project with a small group of participants.

Statistical considerations and power calculation In the questionnaire survey the investigators expect a cohort of approximately 3500 patients.

Here is performed an overall statement of self-reported complications, quality of life and symptoms of dumping partially based on validated scales and partly from questionnaire designed specifically for this study.

Risks, side effects and disadvantages In the questionnaire survey, participation neither is associated with risks, side effects or disadvantages apart from a small time consumption associated with completing the questionnaire.

Respect for the subjects' physical and mental integrity The project is reported to the region's joint notification to the Danish Dataprotection Agency. We hereby declare that the project is carried out in accordance with the protocol and applicable regulatory / legislative.

The Act on Processing of Personal Data will be respected. The study will also be reported to the Clinical Trials and conducted in accordance with the Helsinki Declaration II.

Publication of results Both positive, negative and inconclusive results will be published and sought to be published in English-language, peer-reviewed journals as original publications and with the PhD student as first author.

Perspectives The investigators expect to identify positive and negative consequences for GYP and thus optimize the basis on which patients and physicians in the future will be able to decide on surgery. This will also better prevention of complications and thus save patients and communities of loss, economic as well as social and personal. The project will hopefully form the basis for the continuation of longer follow-up studies. Moreover, the results set the stage for the development of new more "gentle" obesity surgery.

Being tested
Gastric bypass operation
Keywords
Bariatric surgery, Quality of life, Complications

What participants receive

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

  • Gastric bypass operationProcedure or surgery

Study groups in NCT01930851
Study groupRoleWhat they receive
Gastric bypassAll gastric bypass operated patients in the Central Denmark Region 2006-2011
Receives: Procedure: Gastric bypass operation

What is being measured

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

  1. Quality of life

    Measured: 2-7 years

Secondary outcomes (1)
  1. Selfreported complications

    Measured: 2-7 years

Timeline

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

  1. First posted29 Aug 2013 (estimated)
  2. Study startFeb 2014
  3. Primary completionAug 2014
  4. Study completionAug 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
Retrospective
Enrolment
1,429 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01930851
Sponsor's protocol ID
1-16-02-139-13
Status last verified
Aug 2013
First submitted
19 Aug 2013
Last updated
5 Dec 2014
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Complications After Gastric Bypass Operation, run by University of Aarhus 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 2 inclusion and 1 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 5 Dec 2014. 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?

Quality of life (time frame: 2-7 years). 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 5 Dec 2014.

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