Is the transdermal fentanyl patch an efficient way for acute postoperative pain control?

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002221

Enrollment

Registered

2017-02-10

Start date

2015-10-19

Completion date

Unknown

Last updated

2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others : The patients in Group TFP received a single TFP (25 µg/hour fentanyl patch) affixed to the anterior chest wall 14 hours before surgery and Group PCA received a placebo patch in the same manne

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) patients age :between 20 and 80 years of age 2) scheduled for elective laparoscopic cholecystectomy under general anesthesia 3) having an American Society of Anesthesiologists (ASA) physical status of I–II 4) being able to use an IV-PCA.

Exclusion criteria

Exclusion criteria: 1) were pregnant or breastfeeding, 2) had a history of allergy to fentanyl 3) had a contraindication for general anesthesia 4) had major organ diseases 5) had a history of drug abuse

Design outcomes

Primary

Measure	Time frame
fentanyl concentration	—

Secondary

Measure	Time frame
pain score, incidence of nausea, vomiting, respiratory depression, rescue analgesics use	—

Countries

Korea, Republic of

Contacts

Public ContactJiSu Jang

Hallym University Medical Center- Chuncheon

jisu@hallym.or.kr+82-33-240-5594

Outcome results