ClinicalTrials.Veeva

Menu

Reducing Inflammatory Syndrome in Surgery - Colorectal (RISIS-CR) Trial

N

National University Health System (NUHS)

Status and phase

Enrolling
Phase 3

Conditions

Colorectal Cancer

Treatments

Dietary Supplement: Alpha-ketoglutarate
Dietary Supplement: Placebo
Other: Standard care

Study type

Interventional

Funder types

Other

Identifiers

NCT06646809
2022/00724

Details and patient eligibility

About

The study proposes to identify inflammatory responsiveness of patients prior to CRC surgery and administer prophylactic anti-inflammatory treatment targeted only to those with an excessive pro-inflammatory response. The study team believe this to be a creative approach as the principles of personalized medicine will be used to treat the appropriate patients, and equally as importantly, to not further suppress the inflammatory response of those who have poor immune function already.

Geroprotectors reduce inflammation, and may reduce postoperative SIR and complications after CRC surgery. In this proposal, we intend to use alpha ketoglutarate (AKG), a geroprotector supplement that enjoys a GRAS (generally regarded as safe) status with the FDA. [12] Apart from reducing inflammation and inhibiting the mTOR pathway, AKG also prevents loss of muscle mass, improves brain oxygenation, has cardioprotective effects, and improves renal function. It also has anti-cancer effects beyond mTOR pathway inhibition, including regulating HIF-1 activity, suppressing secretion of angiogenic factors, and regulating epigenetic processes.

Full description

The incidence of colorectal cancer (CRC) increases exponentially with age, with >50% of CRC first diagnosed at 50 years or older. Surgery is the mainstay of treatment. However, older patients are more likely to develop postoperative ileus and anastomotic leak, longer hospital stays and higher mortality. In the long-term, they are more likely to experience fatigue and slow recovery.

Surgery triggers an inflammatory response. In some cases, the immune system is unable to distinguish between the stimuli of major surgery (ideally a modest response) and trauma or infection. This overshoot manifests as a postoperative systemic inflammatory response (SIR) and may lead to tissue destruction and organ dysfunction. In CRC surgery, SIR as defined by C-reactive protein (CRP) elevation is associated with postoperative Clavien-Dindo grades III and IV complications where intervention is needed. These complications include infection and anastomotic leak, and are linked to reduced overall survival independent of both surgery-related complications and tumour stage. In addition, preoperative systemic inflammation is a marker of poor prognosis. As ageing is often accompanied by a chronic low-grade inflammation, it was not surprising that preoperative systemic inflammation is more common in older patients.

The use of anti-inflammatory drugs to reduce SIR has had mixed successes. Chronic steroid use is a recognized risk factor for anastomotic leak, but in a recent meta-analysis, the use of preoperative corticosteroids lowered markers of SIR and reduced postoperative infective complications. Similarly, although NSAIDs have been shown to reduce hospital stay and hasten recovery in bowel function, a recent meta-analysis indicated that it increases the risk of anastomotic leaks.

Older patients may have impaired immune response to surgical stress from immunosenescence but conversely, some may develop a more intense and prolonged response. In a population study of elderly people, this heterogeneity conferred a survival benefit to those who could mount a pro-inflammatory response, whereas those with poor pro-inflammatory response were more prone to infections. Therefore, suppressing the postoperative SIR in pro-inflammatory patients is likely beneficial but not in patients with low pro-inflammatory potential.

Enrollment

80 estimated patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged at least 45 years old
  • Undergoing elective colorectal cancer surgery
  • Able to give informed consent

Exclusion criteria

  • Undergoing emergency colorectal cancer surgery
  • Unable to give informed consent
  • Females who are pregnant
  • Cognitively impaired patients

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

80 participants in 3 patient groups, including a placebo group

Low inflammatory responder
Other group
Description:
Low inflammatory responder group - to receive standard care
Treatment:
Other: Standard care
High inflammatory responder - AKG
Experimental group
Description:
High inflammatory responder group - to receive AKG tablets (1g a day, once a day, taken orally)
Treatment:
Dietary Supplement: Alpha-ketoglutarate
High inflammatory responder - placebo
Placebo Comparator group
Description:
High inflammatory responder group - to receive placebo tablets (1g a day, once a day, taken orally)
Treatment:
Dietary Supplement: Placebo

Trial contacts and locations

4

Loading...

Central trial contact

Lian Kah Ti

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems