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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01320319
Other study ID # 11005
Secondary ID
Status Recruiting
Phase Phase 2/Phase 3
First received March 2, 2011
Last updated December 3, 2012
Start date March 2011
Est. completion date March 2013

Study information

Verified date December 2012
Source University of Nottingham
Contact John Williams, MD, FRCS
Phone +44 1332 785566
Email john.williams7@nhs.net
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Interventional

Clinical Trial Summary

Primary Aim is to test the Hypothesis: Nutritional supplementation with 960mg EPA three times a day positively affects muscle function and mass (assessed by muscle biopsies, assays of cellular aerobic function and DEXA scan) and inflammation (measuring cellular markers of inflammation) in patients undergoing resection of colorectal cancers.

The secondary aim is to evaluate aerobic performance assessed by cardiopulmonary exercise testing (CPEX) and perioperative outcome in patients with colorectal cancer post surgical resection.


Description:

Cancer is well documented to cause weight loss and cachexia (1). An inflammatory process driven by the presence of a tumour, can result in reduced food intake (2), increased metabolic output (3) and loss of skeletal muscle (1). They have reduced fitness and feeling of lethargy that affects activities of daily living and quality of life. The process explaining this is not well understood but thought to be due to diminished skeletal muscle mass and performance. When cancer patients undergo surgery, the trauma of surgery, entails an inflammatory process that furthermore leads to more of the above (4). Reducing this inflammatory insult would positively impact fitness, ability to respond to infections, affect length of stay in hospital, recovery from surgery and quality of life following surgery.

Eicosapentaenoic acid (EPA) is an omega-3-fatty acid, derived from fish oil and a commonly available nutritional supplement. It is believed to reduce the inflammatory effect of cancer and the trauma of surgery, in turn dampening the catabolic effect causing skeletal muscle loss. Studies on oesophageal cancer patients have previously suggested that EPA can preserve lean muscle mass (5). The investigators expect EPA to cause less lean muscle loss and improved aerobic performance. High dietary intake is not thought to have health risks (6) and EPA has recently been trialed in infant milk formulas with no adverse effects (7).

The investigators plan to recruit patients from colorectal clinic, who are due to have surgery for colorectal cancer, and give them EPA or placebo, from 5 days prior to surgery to up to 21 days following surgery. The investigators would like to measure markers of muscle function and inflammation, muscle mass, exercise performance on by cardiopulmonary exercise testing, muscle biopsy and muscle grip strength on a dynamometer.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date March 2013
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Colorectal cancer patients listed for open curative tumour resection by means of: Right Hemi Colectomy, Left Hemi-colectomy or Anterior Resection, not having neo-adjuvant chemotherapy.

- Aged 18 - 85 years old.

Exclusion Criteria:

- Strenuous exercise 48 hours before the preoperative assessment.

- Intramuscular injections within 48 hours of any study day.

- Known peripheral neuropathy or myopathy.

- Patients with mobility problems, wheelchair bound or have suffered a previous cerebro-vascular accident with residual impairment of mobility.

- Patients with major/ minor trauma (Motor vehicle accidents or ground falls, firearm injury, drowning, struck by and against injuries).

- Pregnant women. Pregnancy test will be done at the beginning of the study day.

- Patients without mental capacity to give signed consent.

- Patients already taking fish-oil derived nutritional supplement.

- Patients with impaired oral intake.

- Patients known to have metastatic disease.

- Patients having neoadjuvant chemotherapy prior to resection, which may confound results.

- Patients having laparoscopic procedures.

- Patients identified having cardiorespiratory comorbidity considered unsuitable for surgery: unstable angina, myocardial infarction within last 3 months, severe aortic stenosis, pulmonary hypertension, HOCM, acute myopericarditis, chronic heart failure New York Heart Association class 3 and above and impaired left ventricular ejection fraction (less than 43%). Respiratory contraindications include severe COPD, emphysema, fibrosing alveolitis, Interstitial lung disease and FEV1 less than 1.5.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Other:
Placebo
Capsule form, 960 mg to be taken three times a day.
Dietary Supplement:
Experimental: Nutritional Supplementation with EPA
Capsule form, EPA, 960mg to be taken three times a day.

Locations

Country Name City State
United Kingdom School of Graduate Entry Medicine & Health, Royal Derby Hospital Derby

Sponsors (2)

Lead Sponsor Collaborator
University of Nottingham Derby Hospitals NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Nutritional supplementation with 960mg EPA three times a day positively affects muscle function and mass Muscle function and mass will be assessed by muscle biopsies, assays of cellular aerobic function and DEXA scan and inflammation (measuring cellular markers of inflammation). Baseline and 6 weeks post-op No
Secondary The secondary aim is to look at the aerobic performance. The secondary aim is to look at the aerobic performance assessed by cardiopulmonary exercise testing (CPEX) and perioperative outcome in patients with colorectal cancer post surgical resection. Baseline and 5 weeks post-op. No
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