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Non-invasive Monitor in Endoscopic Invasive Procedure

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National Taiwan University

Status

Completed

Conditions

Cholangiopancreatography, Endoscopic Retrograde
Endoscopic Ultrasonography

Treatments

Device: Portable Noninvasive Hemodynamic Monitor

Study type

Observational

Funder types

Other

Identifiers

NCT03292627
201612030RINA

Details and patient eligibility

About

Investigators include the patients who need painless invasive endoscopic procedure, investigators collect the demographic data and apply the non-invasive device ICON on participants during the who procedure.

Full description

Invasive endoscopy procedure including Endoscopic Retrograde Cholangio-Pancreatography (ERCP), endoscopic ultrasound guided fine needle aspiration (EUS-FNA), Endoscopic Retrograde Biliary Drainage (ERBD) and others is more and more popular which become the standard treatment before surgical intervention. However; the elder group who need this procedure is getting more common. The painless endoscopic sedation for elder group who has more comorbidity is not easy. During the procedure, the investigators found that the anticholinergic medication-buscopam which in order to suppress intestine mobilization can cause obvious tachycardia. Tachycardia makes the stroke volume decrease which enhance the perioperative hypotension, and the vasodilation effect of the analgesics make it worse.

Investigators are trying to find the non-invasive predictor of perioperative hypotension in geriatric group. Investigators collected the patients who need painless endoscopic invasive procedure, investigators will record their hemodynamic data including estimated cardiac output (CCO),index of contractility (ICON),NBP,HR,and saturation. Investigators also add the evaluation of frailty to evaluate the relationship between frailty and perioperative complications.

Enrollment

200 patients

Sex

All

Ages

50+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patient who need painless endoscopic invasive procedures
  • age above 50 y/o

Exclusion criteria

Trial design

200 participants in 2 patient groups

mid age
Description:
mid age: 50-70 years old
Treatment:
Device: Portable Noninvasive Hemodynamic Monitor
old age
Description:
old age: age older than 70 years old
Treatment:
Device: Portable Noninvasive Hemodynamic Monitor

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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