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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02174588
Other study ID # 4-2012-0801
Secondary ID
Status Completed
Phase N/A
First received June 23, 2014
Last updated January 23, 2017
Start date January 7, 2013
Est. completion date February 4, 2015

Study information

Verified date January 2017
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Since introduction in 1989, propofol has gained wide acceptance for sedation during endoscopic procedures. The optimal sedation drug during esophagogastroendoscopy (EGD) is not established. Midazolam and propofol are used for sedation drug. Balanced propofol sedation (BPS) refers to the administration of an opiate, a benzodiazepine, and propofol. In this study, the investigators want to compare the patient satisfaction with EGD following balanced propofol sedation (BPS) versus propofol sedation alone.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date February 4, 2015
Est. primary completion date February 4, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria:

1. over 19 years old, male and female

2. patients who have plan to get esophagogastroduodenoscopy (EGD)

Exclusion Criteria:

1. ASA class III or IV

2. Allergies to propofol, sulfites or eggs

3. patients who had surgery for esophagus, stomach or duodenum

4. inpatients

5. patients who had sleep apnea, gastroparesis or achalasia

6. patients who are taking sedative drugs more than 6 months

7. pregnancy

8. hypotension (systolic pressure less than 90mmHg), bradycardia (pulse rates less than 50 times per minute) or hypoxia (SpO2 less than 90%)

9. psychiatric or neurologic problems (ex. epilepsy or dementia)

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Midazolam + propofol
Midazolam and propofol are used for sedation drug. Balanced propofol sedation (BPS) refers to the administration of an opiate, a benzodiazepine, and propofol.
propofol
propofol are used for sedation drug

Locations

Country Name City State
Korea, Republic of Yonsei university College of Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Other complications rates The safety after EGD following balanced propofol sedation versus propofol sedation alone Within the 1 hour after EGD
Other total dose of the sedation drugs The economy after EGD following balanced propofol sedation versus propofol sedation alone Within the 1 hour after EGD
Other visual analog scale The endoscopist's satisfaction with EGD following balanced propofol sedation (BPS) versus propofol sedation alone Within the 1 hour after EGD
Primary visual analog scale The patient satisfaction with EGD following balanced propofol sedation (BPS) versus propofol sedation alone Within the 24 hours after EGD
Secondary complications rates The recovery time after EGD following balanced propofol sedation versus propofol sedation alone. The safety after EGD following balanced propofol sedation versus propofol sedation alone Within the 1 hour after EGD
See also
  Status Clinical Trial Phase
Completed NCT04621591 - Case Series With Saneso 360° Gastroscope N/A