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Clinical Trials/KCT0003439
KCT0003439
Not yet recruiting
未知

Postoperative Analgesic efficacy of continuous wound INfusion after laparoscopy (PAIN): a randomized, double-blind, placebo-controlled trial

Kangbuk Samsung Medical Center0 sites66 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Kangbuk Samsung Medical Center
Enrollment
66
Status
Not yet recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional Study
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • age between 18 and 65 years,
  • \- American Society of Anesthesiologists physical status (ASAPS) classification I–II,
  • \- absence of pregnancy at the time of surgery

Exclusion Criteria

  • \- allergy to ropivacaine,
  • \- laparoscopic surgery needing \= 3 separate skin incisions,
  • \- history of ventral or incisional hernia, pre\-existing coagulopathy, neurologic or cognitive dysfunction,
  • \- systemic or regional (especially, umbilicus) infection,
  • \- previously taking opioids for chronic pain, or
  • \- inability to accurately express their pain.

Outcomes

Primary Outcomes

Not specified

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