The Difference in Carbon Footprint Between Diagnostic Upper GI Endoscopy in Dyspeptic Patients Versus Therapeutic Upper GI Bleeding

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20-80
SponsorKing Chulalongkorn Memorial Hospital

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

This trial does not accept healthy volunteers

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 population

Dyspepsia patients and non-variceal upper GI bleeding receiving upper GI endoscopy at King Chulalongkorn Memorial hospital and Sawanpracharak hospital, Thailand

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

75 Participants
are grouped into 2 trial groups
Group A: Diagnostic upper GI endoscopy
Group B: Therapeutic upper GI endoscopy

Trial outcomes

Primary outcomes

1

To quantify the carbon footprint of diagnostic endoscopy for dyspepsia and therapeutic endoscopy for peptic ulcer bleeding

The primary outcome is to calculate the carbon footprint produced from diagnostic upper GI endoscopy in dyspepsia patients and therapeutic upper GI endoscopy in peptic ulcer patients, focusing on the carbon footprint produced since the patient enter the endoscopy room until they leave the endoscopy room

Time frame
From enrollment to the time that patients leave the endoscopy room

Secondary outcomes

1

To compare carbon emissions between diagnostic and therapeutic upper GI endoscopy

Time frame
From enrollment to the time that patients leave the endoscopy room
2

To compare emissions across different hemostatic techniques (clips, argon plasma coagulation, bipolar probe), with or without epinephrine.

Time frame
From enrollment to the time that patients leave the endoscopy room
3

To evaluate procedural success rates of bleeding stoppage and adverse events (e.g., perforation, post-procedural sepsis) by different techniques

To evaluate procedural success rates of bleeding stoppage and adverse events (e.g., perforation, post-procedural sepsis) by different techniques (follow up to 30 days after treatment was given to see rate of recurrent bleeding)

Time frame
From enrollment to 30 days after treatment

Other outcomes

Sponsors and contacts

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