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Not yet recruitingNCT07004530Updated Jun 4, 2025

the MCCE vs EGD Trial

An interventional study of Magnetically Controlled Capsule Endoscopy (MCCE) and Esophageal-gastro-Duodenoscopy (EGD) in Anaemia and Acute Coronary Syndrome, sponsored by Chinese University of Hong Kong. Not yet recruiting at 1 site in Hong Kong. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2025-06-04.

Sponsored by Chinese University of Hong Kong · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
238
Allocation
Randomized
Ages
19 Years and older
Sex
All
01

Study summary

Anaemia is common in patients with acute coronary syndrome (ACS) and is associated with significant recurrent bleeding risk and major adverse cardiovascular event (MACE). Esophageal-gastro-Duodenoscopy (EGD) is commonly used as an initial investigation for anaemia but is often non-diagnostic. Magnetically Controlled Capsule Endoscopy (MCCE) being less invasive and with comparable diagnostic accuracy as EGD, might be used as an alternative initial investigation for anaemia in patients with ACS.

Read the detailed description

Anaemia is common in patients with acute coronary syndrome (ACS) and is associated with significant recurrent bleeding risk and major adverse cardiovascular event (MACE). Esophageal-gastro-Duodenoscopy (EGD) is commonly used as an initial investigation for anaemia but is often non-diagnostic. Magnetically Controlled Capsule Endoscopy (MCCE) being less invasive and with comparable diagnostic accuracy as EGD, might be used as an alternative initial investigation for anaemia in patients with ACS.

02

Conditions studied

  • Anaemia
  • Acute Coronary Syndrome

Keywords

  • Capsule Endoscopy
  • Esophago-gastro-Duodenoscopy
03

Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

subjects are patients older than 18 years old with:

  1. the diagnosis of ACS as defined by symptoms of chest pain or shortness-of-breath, abnormal electrocardiogram and positive enzyme, requiring coronary intervention
  2. new-onset anaemia as defined by Hb\<11 g/dL on admission blood taking

Exclusion criteria

Exclusion Criteria:

  1. History of active haematological disease including hemoglobinopathies such as thalassemia, Myelodysplastic syndromes, haematological malignancy, aplastic anaemia, or autoimmune haemolytic anaemia.
  2. Patients with known active gastrointestinal malignancy.
  3. Contraindications for CE: suspected or known gastrointestinal obstruction, stenosis, fistula, diverticula, presence of gastrointestinal obstruction symptoms such as pain or dysphagia; inoperative conditions or refusal to undergo abdominal surgery if required; history of laparotomy, gastric or bowel surgery; presence of metallic implants that is not MRI conditional.
  4. Contraindications for EGD: Possible gastrointestinal perforation, medically unstable patients, patient with known pharyngeal diverticulum, and patients with recent head and neck trauma.
  5. Inability to take 1-month DAPT such as non-deferrable surgery within 1 months, severe allergy or hypersensitivity reaction to aspirin or P2Y12 inhibitors, or patients in whom 1 months DAPT is not indicated.
  6. Patients whose life-expectancy is less than 6 months.
  7. Patients who are pregnant or lactating.
  8. Patients who are unable to give informed consent.
  9. Patients who are in active heart failure or fluid-overload state.
  10. Patients who have chronic renal failure as defined by estimated glomerular filtration rate \<15 ml/min/1.73m2.
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
238 participants (estimated)

Study arms

  • Experimental
    MCCE-first arm

    MCCE will be performed for individuals randomized to MCCE arm within the same hospitalization of ACS diagnosis. The MCCE used in this study is the magnetically controlled capsule endoscopy (MCE, AnPx USA) which is a capsule measuring 28x12mm, and contains a permanent magnet inside its dome. Images are captured and recorded at 2 frames/s. Before the MCCE procedure, subjects will be fasted for 8 hours. Capsule will be swallowed with 10ml of clear liquid. During the MCCE examination, subjects will be asked to drink 500 to 1000ml water on demand. Once inside the stomach, the capsule will be navigated via an external magnetic guidance system to obtain a full view of the stomach. After the gastric examination, the subject wears a portable image recorder for images of duodenum and the rest of the small bowel for about 4 hours

    Procedure: Magnetically Controlled Capsule Endoscopy (MCCE)

  • Experimental
    EGD-first arm

    Conventional EGD with intravenous sedation will be performed for individuals randomized to EGD arm within the same hospitalization of ACS diagnosis by an experienced endoscopist. Similar MLD and Forest ulcer grading will be applied as in MCCE arm. Endoscopic therapeutic procedures will be performed at endoscopist's discretion.

    Procedure: Esophageal-gastro-Duodenoscopy (EGD)

Interventions

  • ProcedureMagnetically Controlled Capsule Endoscopy (MCCE)

    . The MCCE used in this study is the magnetically controlled capsule endoscopy (MCE, AnPx USA) which is a capsule measuring 28x12mm, and contains a permanent magnet inside its dome. Images are captured and recorded at 2 frames/s

  • ProcedureEsophageal-gastro-Duodenoscopy (EGD)

    Esophageal-gastro-Duodenoscopy (EGD) is commonly performed to look for source of bleeding in patients with anaemia. However, from our own analysis and from retrospective studies of EGD in patients with ACS, EGD finding was normal or non-significant in 20-80% patients14-16. Moreover, EGD was associated with non-negligible periprocedural risks in patients with ACS, including death directly attributed to EGD (9.1%; 95% CI 7.6-10.9%), hypotension (24.1%; 95% CI 17.0-32.9%), arrhythmias (8.3%; 95% CI 4.5-15.1%) and recurrent ACS (6.5%; 95% CI 3.2-12.8%)

05

What researchers measure

Primary outcomes

  1. the occurrence of recurrent bleeding

    A bleeding event will be defined according to international consensus by the occurrence of any of the followings: 1) overt bleeding of gastroduodenal origin including fresh hematemesis, bloody nasogastric aspiration, melena after normalization of stool colour, or haematochezia after normalization of stool colour, or 2) bleeding of presumed occult gastrointestinal origin with a documented reduction in haemoglobin concentration of ≥2 g/dl or reduction in the haematocrit by 10% or more from the baseline.

    Time frame: baseline, 30 days

Secondary outcomes

  1. Need for any transfusion

    Need for any transfusion

    Time frame: baseline, 30 days

  2. Any bleeding by Thrombolysis in Myocardial Infarction (TIMI), Bleeding Academic Research Consortium (BARC) and GUSTO definitions

    TIMI flow grade is a method used to assess coronary artery blood flow during and after thrombolytic therapy in patients with acute myocardial infarction. It's a standardized way to grade the degree of reperfusion, ranging from complete occlusion (Grade 0) to complete perfusion (Grade 3). BARC: Type 1: Minimal bleeding, not actionable. Type 2: Clinically evident but minor; requires treatment. Type 3: Significant bleeding, divided into 3A (moderate, requires transfusion), 3B (major, may need surgery), and 3C (critical, such as intracranial bleeding). Type 4: Bleeding related to CABG procedures.

    Time frame: baseline, 30 days

  3. Change in Major adverse cardiac events

    MACE as defined by death of cardiovascular origin, non-fatal myocardial infarction, non-fatal stroke, or clinically driven target vessel revascularization.

    Time frame: baseline, 30 days

  4. Any adverse events and complications from MCCE and/or from EGD

    Any adverse events and complications from MCCE and/or from EGD

    Time frame: baseline, 30 days

06

Study locations

1 site
  • Prince of Wales Hospital
    Hong Kong, Shatin 0000, Hong Kong
07

Registry details

Key details

Study ID
NCT07004530
Lead sponsor
Chinese University of Hong Kong
Collaborators
Health and Medical Research Fund
Responsible party
GuangMing Tan (Assistant professor, Chinese University of Hong Kong) — Principal investigator
First posted
Jun 4, 2025
Start date
Sep 24, 2025 (estimated)
Primary completion
Sep 24, 2027 (estimated)
Completion
Nov 24, 2027 (estimated)
Last update
Jun 4, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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