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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05314725
Other study ID # REG-094-2021
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received
Last updated
Start date June 1, 2022
Est. completion date June 1, 2023

Study information

Verified date March 2022
Source Zealand University Hospital
Contact Emilie Palmgren Colov, MD
Phone +45 61335122
Email eco@regionsjaelland.dk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to investigate the effect of an SGLT-2 inhibitor on postoperative hyperglycemia after acute abdominal surgery in patients without diabetes


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 24
Est. completion date June 1, 2023
Est. primary completion date May 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - - Admitted to the ward after acute abdominal surgery (ASAP patient at Slagelse Hospital, OMEGA patient at Zealand University Hospital) - At least two independent measurements of blood glucose above 7.7mmol/l within the first 48 hours after surgery - Age of 18 to 85 - Must be able to understand and sign informed content Exclusion Criteria: - Patients diagnosed with diabetes mellitus - Impaired kidney function (eGFR < 45mL/min) - Severe liver disease (defined as transaminases above X 3 normal levels) - Acute pancreatitis within the last two months or a history of chronic pancreatitis - Participation in another pharmacological intervention trial - Predictable poor compliance (for instance mentally impaired) - Pregnancy or lactation (fertile women must have a negative serum or urine pregnancy test to participate) - Allergy to study medication

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
SGLT2 inhibitor
10 days of SGLT2 inhibitor after surgery
Placebo
10 days of placebo after surgery

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Zealand University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary time in range percentage of time in range defined as blood glucose between 3.9 and 7.8mmol/l. Blood glucose will be measures continuously while taking the study medication) from inclusion until 10 days after (or when the patient leaves the hospital)
Secondary mean glucose from inclusion until 10 days after (or when the patient leaves the hospital)
Secondary glucose variability standard deviation divided by the mean and standard deviation from inclusion until 10 days after (or when the patient leaves the hospital)
Secondary time with level 1 hypoglycemia blood glucose 3.0-3.9mmol/l from inclusion until 10 days after (or when the patient leaves the hospital)
Secondary time with level 2 hypoglycemia blood glucose less than 3mmol/l from inclusion until 10 days after (or when the patient leaves the hospital)
Secondary time with hyperglycemia blood glucose more than 10mmol/l from inclusion until 10 days after (or when the patient leaves the hospital)
Secondary Quality of recovery-15 Questionnaire assessing the patient's own sense of recovery after surgery every day while taking the study medication and on postoperative day 30
Secondary Nanostring changes in up- and downregulation of genes at inclusion, on day 4 of treatment and at end of treatment
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