No registrations found.
ID
Source
Brief title
Health condition
Diabetes mellitus
Surgery
Anaesthesia
HbA1c
Sponsors and support
Intervention
Outcome measures
Primary outcome
The main outcome parameter is whether it is possible to lower HbA1c > 1mmol/mol in the participating subjects or not.
Secondary outcome
As secondary outcome we will ask the patient to perform a fasting plasma glucose fingerstick measurement in the week of study inclusion and on the day of surgery. Also, complications will be registered for evaluation, although this study will to assess any relation between HbA1c and complications.
Background summary
Rationale: Preoperative HbA1c values are related to the risk of postoperative complications and mortality in patients with diabetes mellitus (DM). Therefore, the effect of preoperative HbA1c lowering on postoperative complications in poorly regulated diabetes mellitus (DM) patients should be evaluated. However, until now it is unknown whether it is possible at all to lower HbA1c in patients awaiting elective surgery.
Objective: To study the feasibility of lowering HbA1c before elective surgery in patients with suboptimally controlled DM (HbA1c >53 mmol/mol).
Study design: We will perform a single-centre open label pilot trial.
Study population: Fifteen adult patients (18-80) with poorly regulated DM type 2, scheduled for elective surgery.
Intervention: All participating subjects will be referred to the in-hospital diabetes nurse (IHDN) for optimisation of their DM treatment.
Main study parameters/endpoints: The main outcome parameter is the proportion of patients in which HbA1c lowering is successful (ie > 10 mmol/mol decrease inclusion-surgery or HbA1c before surgery <53 mmol/mol), comparing HbA1c at inclusion (during pre-assessment) with HbA1c on the day of surgery.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Risk associated with this study is comparable to routinely optimizing diabetes care and thereby lowering HbA1c in the outpatient setting. The main risk is hypoglycaemia, and this will be prevented as much as possible in clinical practice. Possible benefit is improvement of diabetes regulation and reduction in postoperative complications. In general, this study will be the first step towards a randomized controlled trial, studying the possible benefits of lowering postoperative complications in patients with DM.
Study objective
Preoperative HbA1c values are related to the risk of postoperative complications and mortality in patients with diabetes mellitus (DM). Therefore, the effect of preoperative HbA1c lowering on postoperative complications in poorly regulated diabetes mellitus (DM) patients should be evaluated. However, until now it is unknown whether it is possible at all to lower HbA1c in patients awaiting elective surgery within a short time period.
Therefore the objective of this project is to study the feasibility of lowering HbA1c before elective surgery in patients with poorly controlled DM (HbA1c >7%/53 mmol/mol).
Study design
Screening
Patients with DM presenting at the outpatient anaesthesiology pre-assessment clinic will be asked to participate in the study. As standard clinical procedure, blood will be drawn for HbA1c determination for all patients with DM scheduled for surgery. Based on the outcome, patients that have an HbA1c >7% (53 mmol/mol) and are willing to participate will be contacted by the IHDN.
Intervention
The IHDN will evaluate the current DM treatment in a first phone contact. The IHDN will provide a treatment advice to optimise the current treatment, if necessary in cooperation with the patient’s primary care physician or other care providers treating the patient for DM. Follow-up and outpatient visits will be planned if deemed necessary by the IHDN. Optimisation of therapy is patient dependent, but will be performed according to the NHG standard and AMC diabetes protocols.
Day of surgery
Blood will be drawn for HbA1c determination on the day of surgery. A fasting fingerstick glucose measurement is performed.
Intervention
Patients willing to participate and meeting the in- and exclusion criteria will be referred to the in-hospital diabetes nurse (IHDN). The IHDN will contact the patient by phone and evaluate the current DM treatment. The IHDN will provide a treatment advice to optimise the current treatment, if necessary in cooperation with the patient’s primary care physician. Follow-up and outpatient visits will be planned if deemed necessary by the IHDN. Optimisation of therapy is patient depending, but will be performed according to the NHG standard and AMC diabetes protocols. The IHDN is supervised by prof. dr. J.H. DeVries, endocrinologist involved in this study. On the day of surgery, blood will be drawn for a final HbA1c determination.
Inclusion criteria
- Diagnosis of DM type 2 at least 3 months prior to the screening
- Adult patients, age 18-80 years inclusive
- HbA1c >7% (53 mmol/mol) as measured at the pre-assessment clinic
- Scheduled for elective surgery
- Willing and able to provide written informed consent
Exclusion criteria
- Emergency surgery or scheduled surgery < 3 weeks
- Palliative oncological surgery
- Underlying condition that does not allow patients to participate in the study
Design
Recruitment
Followed up by the following (possibly more current) registration
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL6143 |
NTR-old | NTR6298 |
CCMO | NL61715.018.17 |
OMON | NL-OMON44634 |