Actively Recruiting

Age: 18Years - 80Years
All Genders
ID07431983

Prospective Evaluation of the Carbon Footprint and Clinical Utility of Intestinal Bowel Ultrasound Compared to Colonoscopy and Enterography in Ulcerative Colitis and Crohn's Disease

Led by Asian Institute of Gastroenterology, India · Updated on 2026-05-12

200

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Healthcare contributes about 4.4% of global greenhouse gas emissions, with diagnostic imaging and endoscopic services playing a significant role. Colonoscopy and cross-sectional imaging are essential for diagnosing and monitoring Ulcerative Colitis (UC) and Crohn's Disease (CD) but are linked to high carbon emissions due to energy use, waste, sterilization, and transportation. Intestinal Bowel Ultrasound (IBUS) is a non-invasive, real-time diagnostic tool gaining validation for assessing disease activity in UC and CD with a lower environmental impact. This research compares the environmental footprint and clinical usefulness of IBUS against traditional imaging methods like colonoscopy for UC patients and CT/MRI enterography for CD patients. The study observes patients undergoing these procedures in real-world clinical care to quantify electricity and water consumption, waste generation, and greenhouse gas emissions over a 12-month period. Participants provide consent to include their endoscopy procedures during the study period. Researchers will measure environmental impacts and assess the diagnostic value of IBUS compared to standard imaging. The study runs until December 2026 and aims to support more sustainable follow-up methods for inflammatory bowel disease by monitoring resource use and emissions during routine care.

CONDITIONS

Brief Title

Prospective Evaluation of the Carbon Footprint and Clinical Utility of IBUS Compared to Colonoscopy and Enterography in UC and CD

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 80 years
  • Diagnosed with Ulcerative Colitis or Crohn's Disease
  • Undergoing endoscopy procedures during the study period
  • Provide consent for participation
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Up to 12 months

Participants undergo diagnostic procedures including Intestinal Bowel Ultrasound (IBUS) and standard imaging such as colonoscopy or CT/MRI enterography to assess disease activity.

1 to 2 visits depending on disease type and imaging modality

Long-term Monitoring

Duration - Up to 12 months

Participants are observed over time to evaluate the environmental impact and clinical utility of the diagnostic procedures used.

Trial Site Locations

Total: 2 locations

1

AIG Hospitals

Hyderabad, Telangana, India, 500032

Actively Recruiting

2

AIG Hospitals

Hyderabad, Telangana, India, 500032

Actively Recruiting

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Research Team

D

Dr.Hardik Rughwani

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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Published Research Related To This Trial