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A Randomised Double-Blind Multicentre Placebo-Controlled Study to Investigate the Effect of Ranitidine on the Post-Operative Infection Rate and Survival Rate of Patients Undergoing Surgery for Colorectal Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14545665
Enrollment
Unknown
Registered
2002-08-19
Start date
2002-01-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colon, Rectum Cancer Colorectal

Interventions

1. Group A: Intravenous ranitidine, 100 mg, administered twice daily for 5 days or until oral treatment is tolerated, followed by oral ranitidine, 150 mg twice daily until death or for a period of 5 y

Sponsors

Glaxo Wellcome (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Aged >18 years 2. Diagnosis of colorectal cancer 3. This is the first operation for cancer and the life expectancy of the patient is at least 3 months at the time of surgery 4. No concurrent chronic modulating therapy with systemic steroids, antiviral agents or other known immunomodulating drugs 5. No systemic antimicrobial agents in the 48 h prior to entry into the study 6. Not currently or planning to undergo chemotherapy, radiotherapy or any other therapy for cancer 7. No medical contraindications to protocol treatments

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
Not provided at time of registration

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026