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Assessing analgesia in single and repeated administrations of acetaminophen for postoperative pain after gynecologic laparoscopic surgery

Assessing analgesia in single and repeated administrations of acetaminophen for postoperative pain after gynecologic laparoscopic surgery - Repeated vs single administrations of acetaminophen (gynecologic laparoscopic surgery)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000019775
Enrollment
48
Registered
2015-11-16
Start date
2014-10-09
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Ovarian desease

Interventions

Sponsors

Sapporo Medical University, School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients with American Society of Anesthesiologists physical status 1-2 who were scheduled to undergo elective gynecologic laparoscopic surgery under general anesthesia.

Exclusion criteria

Exclusion criteria: 1) Weighed < 40 or > 100 kg 2) Pregnancy 3) Having neurological, cardiovascular, and respiratory complications. 4) Allergy to amide local anesthetics or opioids4 5) Psychoactive medications 6) Hepatic or renal failure 7) Inability to understand the pain scale 8) Not obtained informed consent

Design outcomes

Primary

MeasureTime frame
1) postoperative pain score (numerical rating scale: NRS) at 2, 4 hour at postoperative day (POD) 0, AAM and PM at POD 1 and 2 2) supplemental analgesia for 2 days

Secondary

MeasureTime frame
1) postoperative nausea and vomiting for 2 days 2) satisfaction of the patient using NRS at POD 2

Countries

Japan

Contacts

Public ContactYukitoshi Niiyama

Sapporo Medical University, School of Medicine Department of Anesthesiology

niiyama@sapmed.ac.jp011-611-2111(3568)

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026