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Clinical Trials/KCT0009540
KCT0009540
Completed
未知

Comparison of the effectiveness of local analgesic injection pump devices and local topical gel-type analgesic agents for postoperative pain control in patients undergoing bariatric metabolic surgery: A randomized controlled trial

Seoul National University Bundang Hospital0 sites48 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Endocrine, nutritional and metabolic diseases
Sponsor
Seoul National University Bundang Hospital
Enrollment
48
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
December 20, 2023
Last Updated
last year
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • The study enrolled participants who satisfied the National Health Insurance criteria for bariatric surgery, which necessitates a body mass index (BMI) of \=35 kg/m2 or a BMI of \=30 kg/m2 with associated obesity\-related complications such as hypertension, hyperlipidemia, diabetes, fatty liver and polycystic ovary syndrome. And individuals aged 19 years or older who voluntarily consented to participate in the study were included.

Exclusion Criteria

  • The exclusion criteria included: 1\) Patients who were currently receiving, or had previously received, any investigational products, or those with medical conditions that could affect the safety and efficacy evaluation of this medical device; 2\) Patients with known hypersensitivity to ropivacaine or other amide\-type local anesthetics; 3\) Patients experiencing severe bleeding or shock; 4\) Patients with inflammation at or around the site of injection; 5\) Patients suffering from sepsis; 6\) Patients requiring intravenous partial anesthesia; 7\) Patients who had participated in another clinical study within the past 30 days; 8\) Patients considered unsuitable by the investigator for various reasons, such as lack of cooperation; and 9\) Patients with contraindications to using ketorolac.

Outcomes

Primary Outcomes

Not specified

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