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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03152617
Other study ID # MWerling
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 2015
Est. completion date December 2027

Study information

Verified date September 2019
Source Göteborg University
Contact Lars Fandriks, M.D., PhD.
Phone +46313424123
Email lars.fandriks@gastro.gu.se
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Weight-reducing obesity surgery (OS) generally gives good results but complications are common; e.g. impaired weight loss, weight regain, bowel pain, diarrhea, vitamin/mineral deficiency, osteoporosis and impaired dental health. The BASUN study is a prospective 10-year comparison of 1000 surgically and 400 conventionally treated individuals regarding adverse side-effects, risk factors for complications and poor outcome.


Description:

The use of obesity surgery (OS) has increased dramatically due to the lack of effective conventional weight reducing methods. OS generally gives a sustained weight reduction and improves metabolic co-morbidities but complications are not uncommon, e.g. weight regain, bowel pain, diarrhea, vitamin/mineral deficiency, osteoporosis and impaired dental health. Studies of OS regarding adverse side-effects, risk factors for complications and poor outcomes are few or missing.

The BASUN study is a prospective 10-year comparison of 1000 surgically and 400 conventionally treated individuals. Inclusion started in April 2015 and will be completed in 2017. Subjects are consecutively included from the whole western region of Sweden and are followed by detailed checkups at 2, 5 and 10 years. Protocol includes nutritional and bone status, oral health, psychiatric health, GI symptoms, socioeconomics and health economy. Data are collected by interviews, blood and fecal samples, questionnaires, dual energy x-ray absorptiometry, dentist examinations, patients' record and registries. The study is carried out in close cooperation with experts in surgery, medicine, psychiatry, endocrinology, gastroenterology, hematology, molecular biology, osteoporosis, oral medicine, physiology and general medicine.

The BASUN study will be able to form the basis for more individualized medical guidelines with the objective of improving therapeutic quality and the utilization of health care resources.


Recruitment information / eligibility

Status Recruiting
Enrollment 1400
Est. completion date December 2027
Est. primary completion date April 2027
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All patients eligible for obesity treatment under specialist care with medical methods or with surgery

Exclusion Criteria:

- no ability to speak, read or write in Swedish

Study Design


Locations

Country Name City State
Sweden Department of Gastrosurgical R & E, the Sahlgrenska Academy,University of Gothenburg Göteborg

Sponsors (1)

Lead Sponsor Collaborator
Göteborg University

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Other Nutritional status Blood biochemistry package: Retinol, RBP, Vitamins B, Vid D, methylmalonate, homocysteine, hemoglobulin, MCV, MCH, MCHC, reticulocytes, iron, transferrin, ferritin , Zn, S-Albumin, creatinine, blood lipid profile, ALP; reported value will be number of patients with one or more abnormal laboratory value(-s). 2, 5 & 10 years
Other Psychomorbidity1: Depression Patient Health Questionnaire 9 (PHQ-9); reported value: number of (or percentage) patients reporting scores indicating a moderate to severe depressive state 2, 5 & 10 years
Other Psychomorbidity2: Anxiety Beck Anxiety Inventory (BAI); reported value: number of (or percentage) patients reporting high scores indicating moderate to severe anxiety 2, 5 & 10 years
Other Psychomorbidity3: Adult ADHD Adult ADHD Self-Report Scale -Screener (ASRS); reported value: number (or percentage) of patients reporting scores above cut-off indicating adult ADHD symptoms 2, 5 & 10 years
Other Psychomorbidity4: Drug use Drug Use Disorders Identification Test (DUDIT); reported value: number (or percentage) of patients reporting scores above cut-off indicating risk for drug-related problems 2, 5 & 10 years
Other Psychomorbidity5: Alcohol Alcohol Use Disorders Identification Test (AUDIT); reported value: number (or percentage) of patients reporting scores above cut-off indicating risk for alcohol-related problems 2, 5 & 10 years
Other Gastrointestinal symptomatology Rome III Diagnostic criteria; reported value: number (or percentage) of patients fulfilling the criteria for functional gastrointestinal gastrointestinal disorder 2, 5 & 10 years
Other Oral Health questionnaire Oral Health Impact Profile (OHIP-14); reported value: number (or percentage) of patients scoring above cut-off for oral health impacting quality of life. 2, 5 & 10 years
Primary Ionized Calcium in serum Difference between pre- and posttreatment level; unit: mM 10 years
Secondary Bone mineral density (BMD) DXA based assessment; units: areal density (g/cm2) 10 years
Secondary Bone mineral density (T-score) T-score is bone mineral density (BMD)in relation to young healthy adults of the same sex; unit: number of standard deviations below or above BMD of controls 10 years
Secondary Bone mineral density (Z-score) Z-score is bone mineral density (BMD) in relation adults of the same age; unit: number of standard deviations below or above BMD of controls of the same age 10 years
Secondary Arterial blood pressure arterial systolic and diastolic pressure at rest; mmHg 2, 5 & 10 years
Secondary Quality of Life 36-item Short Form Survey(RAND36); Reported value: reported value: number of (or percentage) patients reporting physical and mental health summary scores indicating moderately to severely reduced quality of life as compared to a general reference population. 2, 5 & 10 years
Secondary Plasma Glucose Concentration Fasting value; unit: mM 2, 5 & 10 years
Secondary Serum Insulin Concentration Fasting value; unit: mIE/L 2, 5 & 10 years
Secondary Glycated Hemoglobin (HbA1c) Unit: mmol/mol 2, 5 & 10 years
Secondary Change in Body Weight From Baseline kg 2, 5 & 10 years
Secondary Change in Body Mass Index (BMI) kg x m2 2, 5 & 10 years
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