Clinical Trials Directory

Trials / Unknown

UnknownNCT04412421

Supplementation After Bariatric Surgery

Adherence to Vitamin and Mineral Supplementation After Bariatric Surgery

Status
Unknown
Phase
Study type
Observational
Enrollment
260 (actual)
Sponsor
Region Östergötland · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to assess medication adherence to vitamin and mineral supplements after bariatric surgery and identify factors that may influence adherence. All study participants are prescribed life-long treatment with daily oral vitamin B12 and Calcium/Vitamin-D. Menstruating women are also prescribed daily oral iron supplementation. Post-operative adherence rate is retrieved from Pharmacy refill data, collected from the Swedish Prescribed Drug Register, the five first years after bariatric surgery.

Detailed description

The aim of this study is to assess medication adherence to vitamin- and mineral supplementation after bariatric surgery, identify factors that may influence adherence, as well as study the development of micronutrient deficinencies detectable by blood sampling. All study participants are prescribed life-long treatment with daily oral vitamin B12 and Calcium/Vitamin-D. Menstruating women are also prescribed daily oral iron supplementation. Post-operative adherence rate is retrieved from pharmacy refill data, collected from The Swedish Prescribed Drug Register, at one, two and five years after bariatric surgery.

Conditions

Interventions

TypeNameDescription
PROCEDUREGastric Bypass, Sleeve GastrectomyLifelong vitamin and Mineral supplementation

Timeline

Start date
2017-05-03
Primary completion
2020-07-01
Completion
2023-07-01
First posted
2020-06-02
Last updated
2020-06-02

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT04412421. Inclusion in this directory is not an endorsement.

Supplementation After Bariatric Surgery (NCT04412421) · Clinical Trials Directory