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Hem-col® as an alternative for standard laboratory testing in the follow up of patients after bariatric surgery

Hem-col® as an alternative for standard laboratory testing in the follow up of patients after bariatric surgery - The Hem-Col Study

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON46649
Enrollment
100
Registered
2018-03-17
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

obesitas overweight

Interventions

None listed

Sponsors

Slotervaartziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: -Patients who have undergone a laparoscopic roux and y gastric bypass, laparoscopic omega loop gastric bypass, laparoscopic redo gastric bypass, laparoscopic gastric sleeve, laparoscopic distal gastric bypass or laparoscopic duodenal switch. -Patients having a routine blood check after 6 months or for the routine annual check. -Informed consent to participate.

Exclusion criteria

Exclusion criteria: None.

Design outcomes

Primary

MeasureTime frame
The main study parameter will be the difference in levels of different blood parameters between the two tested methods. The levels of the following blood parameters will be studied: Hemoglobin, C-reactive protein, creatinine, calcium, cholesterol, triglycerides, glucose, Hemoglobin A1c, thyroid stimulating hormone, vitamin B1, vitamin B6, folic acid, vitamin B12, vitamin D, ferritin, parathyroid hormone.—

Secondary

MeasureTime frame
NVT.—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)