Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT07171853

The Carbon Footprint Study of Colonoscopy

Led by King Chulalongkorn Memorial Hospital · Updated on 2025-09-18

150

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

With global warming intensifying, GI endoscopy is among the top three greenhouse gas-emitting medical procedures. Colonoscopy, a cornerstone for colorectal cancer (CRC) screening, significantly contributes to the carbon footprint (CF). This study quantifies CO₂ emissions in different steps of colonoscopy and evaluates the environmental impact of common polypectomy techniques to establish baseline CF data and identify opportunities for mitigation. This study included patients undergoing colonoscopy for CRC screening. CO₂ emissions were comprehensively measured at each step of the procedure (pre-, during, and post-colonoscopy), including energy consumption, all equipment and medications, waste management, and endoscopy reprocessing. Emission data were also collected for common polypectomy techniques, including cold forceps biopsy (CFB), cold snare polypectomy (CSP), hot snare polypectomy (HSP), and hot snare endoscopic mucosal resection (EMR), all performed according to standard polypectomy protocols.

CONDITIONS

Official Title

The Carbon Footprint Study of Colonoscopy

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18-80 years
Not Eligible

You will not qualify if you...

  • Patient status grade III-V according to the American Society of Anesthesiologists (ASA)
  • Poor bowel preparation (grade <6 in the Boston Bowel Preparation Scale [BBPS])
  • Endoscopic JNET type III or suspicion of malignancy
  • Hematologic or coagulation disorders, platelet count <140,000/mcL, INR >1.5
  • Anti-platelet or anticoagulant medication that cannot be paused as recommended in current guidelines
  • Emergency colonoscopy, gastrointestinal bleeding, unstable vital signs, or critically ill patient
  • Inflammatory bowel disease
  • Pregnancy
  • Severe cardiopulmonary disease
  • Severe infection
  • Malignancy
  • History of allergy to intravenous sedative medication

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

King Chulalongkorn Memorial Hospital

Bangkok, Bangkok, Thailand, 10330

Actively Recruiting

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Research Team

P

Phubaet Washrawirul, Medical

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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