CARBEX: Role of Preoperative Carbohydrates Drinks, Dichloroacetate and Exercise on Postoperative Muscle Insulin Resistance

Sponsor
University of Nottingham (Other)
Overall Status
Unknown status
CT.gov ID
NCT02469337
Collaborator
(none)
40
1
4
61
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Study Details

Study Description

Brief Summary

The aim of the study is to investigate whether preoperative interventions such as carbohydrate drinks, Dichloroacetate and exercise would inhibit or reverse the changes in molecular mechanisms regulating muscle carbohydrate oxidation and postoperative muscle insulin resistance in patients undergoing major abdominal surgery.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

Forty patients undergoing open elective gastrointestinal surgery, will be randomized to four groups of 10 each. The patients will be randomised to receive either preoperative (1) oral carbohydrate drinks (CHO) or (2) infusion of Dichloroacetate with oral carbohydrate drinks (3) exercise or (4) standard care.

Since the interventions are qualitatively different and only the physiological mechanisms are being studied rather than the clinical outcomes, the study is not blinded and no placebo is used.

Analysis for cytokines, insulin, glucagon levels will be performed at screening, during surgery and on the 2nd postoperative day. Muscle biopsies will be taken at the beginning and end of surgery, from rectus abdominus and vastus lateralis muscles for analysis of mRNA (IL-6, TNF-α, Akt1, IRS-1, FOXO1, MAFbx, MURF1 and PDK4) and protein (MafBx, FOXO1, PDK4) expression and muscle metabolites (glycogen, lactate, triglycerides and FFA). Oral Glucose Tolerance Test (GTT) to be performed at the screening visit and on the 2nd postoperative day using a standard protocol. The techniques to be employed to study the above will include RT-PCR, radioimmunoassay, spectophotometry, bioluminometry, Western blotting and ELISA.

Primary outcome: The changes in indices of muscle insulin resistance and muscle protein breakdown at the beginning and at the end of surgery, in response to surgical stress.

Secondary outcomes: (a) The expression of muscle metabolites, reflecting muscle protein turnover (b) Clinical Outcomes: Length of stay and incidence of postoperative complications.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Randomized Control Trial of Dichloroacetate, Preoperative Carbohydrate Loading and Moderate Intensity Exercise on Muscle Insulin Resistance After Major Abdominal Surgery
Study Start Date :
May 1, 2012
Anticipated Primary Completion Date :
Jun 1, 2017
Anticipated Study Completion Date :
Jun 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Preoperative carbohydrate drinks

Patients who were randomised to carbohydrate group ingested 800ml PreOp (Nutricia Clinical Care, 12.5g CHO/100 ml) the night before and 400ml in the morning of surgery, about 2-3 hours before the induction of anaesthesia.

Dietary Supplement: Carbohydrate drinks
preoperative carbohydrate drinks

Active Comparator: Dichloroacetate infusion

The patients in the dichloroacetate group received the CHO drinks as well as an intravenous infusion of DCA (50mg/kg body weight) over 45 min, one- two hours before the induction of anaesthesia.

Drug: Dichloroacetate
Dichloroacetate, an analog of acetic acid has been shown to increase the activation of PDC by inhibiting PDK4 in humans. This drug is expected to shift the metabolism of pyruvate from glycolysis and towards oxidative pathway in the mitochondria
Other Names:
  • sodium dichloroacetate
  • Active Comparator: Moderate intensity exercise

    Patients randomised to exercise group, will perform a 30 min exercise using a semi-recumbent exercise bike, at about 70% of their age estimated heart rate(determined by the formula: (220-Age)*0.7 under close supervision and monitoring of their vital parameters.

    Behavioral: Moderate intensity exercise
    30 min exercise using a semi-recumbent exercise bike, at about 70% of their age estimated heart rate

    No Intervention: Control

    Patients in this group will have surgery as standard practice with none of the above interventions

    Outcome Measures

    Primary Outcome Measures

    1. insulin resistance [48 hours after surgery]

      Relative changes in indices of muscle insulin resistance namely PDC activity, PDK4 mRNA and protein expression.

    Secondary Outcome Measures

    1. muscle carbohydrate oxidation [48 hours after surgery]

      Changes in muscle metabolites such as glycogen, glucose, lactate, reflecting the changes in skeletal muscle carbohydrate oxidation.

    2. Mitochondrial ATP production [48 hours after surgery]

      Mitochondrial ATP production rates in patients undergoing major abdominal surgery.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • All patients over 18 years of age, who are undergoing major elective open abdominal surgery will be included in the study. Patients should be able to provide a written informed consent to participate in the study.
    Exclusion Criteria:
    • Patients who are
    1. Undergoing emergency surgery

    2. Suffering from chronic illness, (e.g. diabetes) or other debilitating diseases

    3. On long term anti-inflammatory drugs, (e.g. NSAIDS, Steroids, immunosuppressant)

    4. On long term antibiotics

    5. On Statins

    6. On full therapeutic dose of anticoagulants, or aspirin >325 mg/day, Clopidrogel

    75mg/day

    1. Suffering from bleeding diathesis

    2. Unable to give consent

    3. Pregnant or breastfeeding.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Hospitals Nottingham Queen's Medical Centre Nottingham United Kingdom NG7 2UH

    Sponsors and Collaborators

    • University of Nottingham

    Investigators

    • Principal Investigator: Dileep N Lobo, Professor, University of Nottingham

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Nottingham
    ClinicalTrials.gov Identifier:
    NCT02469337
    Other Study ID Numbers:
    • 11/EE/0395
    First Posted:
    Jun 11, 2015
    Last Update Posted:
    Jan 5, 2017
    Last Verified:
    Jan 1, 2017
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 5, 2017