About this trial
The goal of this observational study is to learn about the carbon footprint produced from diagnostic upper GI endoscopy in patients with dyspepsia and therapeutic upper GI endoscopy in patients with non-variceal upper GI bleeding. The main question it aims to answer is:
• How much carbon footprint is generated from upper GI endoscopy Participants are already receiving diagnostic and therapeutic upper GI endoscopy as part of their regular medical care for dyspepsia and non-variceal upper GI bleeding, respectively. The carbon footprint generated from this treatment process is examined.
Eligibility criteria
Qualifiers
Patients with dyspepsia or non-variceal upper GI bleeding
Age 20-80 years
Body mass index of 30 or less;
Disqualifiers
Platelet < 50,000
INR > 2.5
Pregnancy
History of allergy to IV sedative medication
Trial design
Treatments tested in this trial
- Not listed