Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03430440
Other study ID # 4-2016-1152
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 1, 2017
Est. completion date November 11, 2020

Study information

Verified date January 2019
Source Yonsei University
Contact Ki Young Lee, MD
Phone 82-02-2228-73997
Email KYLEE504@yuhs.ac
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Epidural PCA (patient controlled analgesia) for post-operative pain management are effective analgesic method. It is widely used in the postoperative pain management for decades.

PCA pumps typically set a fixed basal infusion rate to infuse the analgesics at a constant rate per every hour (conventional mode). In contrast, the newly developed computer-integrated patient-controlled analgesia (CIPCA) mode increases or decreases the basal infusion rate with the use of the patient's bolus button. The CIPCA mode sets the basal infusion rate, the increase / decrease rate of basal rate, and the increment / decrement interval. If the patient presses the bolus button within the set time interval, the set infusion rate is increased because the analgesic is more required. If the bolus button is not pressed during the set time interval, the infusion rate is decreased. Therefore, it can be said that it is an effective method to control the dose of analgesic agent more sensitively to changes in patient's needs and pain.


Recruitment information / eligibility

Status Recruiting
Enrollment 76
Est. completion date November 11, 2020
Est. primary completion date November 11, 2020
Accepts healthy volunteers No
Gender All
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria:

1. elective open gastrectomy due to stomach cancer

2. ASA classification ?-?

Exclusion Criteria:

1. hematologic clotting defect

2. sepsis

3. distance metastasis

4. PCA drug (fentanyl, Ropivacaine) allergy

5. Patients who can not read the consent form or are not fluent in Korean (illiterate, foreigner)

6. pregnant, lactating women

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Apply CIPKA mode
The newly developed computer-integrated patient-controlled analgesia (CIPCA) mode increases or decreases the basal infusion rate with the use of the patient's bolus button. Compared with the conventional mode in which only the basal infusion rate is set to be fixed, the CIPCA mode sets the basal infusion rate, the increase / decrease rate of basal rate, and the increment / decrement interval.
Conventional mode
PCA pumps typically set a fixed basal infusion rate to set the analgesic to enter at a constant rate every hour (conventional mode).

Locations

Country Name City State
Korea, Republic of Severance Hospital 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
Primary Postoperative pain (numerical rating scale: 0 ~ 10) at 6 hours postoperatively
Secondary Postoperative pain (numerical rating scale: 0 ~ 10) at 1, 24, and 48 hours after surgery
Secondary PCA total dose/additional analgesic dose at 1, 6, 24, 48 hours after surgery
Secondary Side effects of PCA (area and vomiting / hypotension / muscle weakness at 1, 6, 24, 48 hours after surgery