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Opioid Use After Laparoscopic Salpingectomy

StatusRecruiting
PhasePhase 4
Started2024-04-25
View on ClinicalTrials.gov ↗

Amendment history

2026-06-01
Study Status, Study Description, Study Design v3
Enrollment target120→38
Study description+449 characters
This study is designed as a non-inferiority trial comparing a non-opioid post-operative pain control regimen to the standard opioid pain control regimen for post-operative salpingectomy patients. A non-inferiority margin of 2 units was selected, such that the experimental treatment will be considere [...]
2025-11-10
Study Status v2
Primary completion date2025-11→2026-11
Completion date2026-01→2026-11
2025-05-15
Study Status, Oversight, Study Design v1
PhaseNot applicable→Phase 4
Primary completion date2025-05→2025-11
Completion date2025-06→2026-01
2024-05-23
Original filing
The purpose of this study is to evaluate patient-reported post-operative pain scores following minimally invasive tubal sterilization procedures to determine if a multimodal, non-opioid pain control regimen is non-inferior to a pain control regimen including opioids. The study team hypothesizes that with extensive counseling on pain management, multimodal medication use, and expectation with non-opioid methods can effectively eliminate the need for opioid prescriptions after laparoscopic salpingectomy.
Trial Details
NCT Number NCT06434233
Lead Sponsor Johns Hopkins University
Conditions Opioid Use, Post-operative Pain, Sterility, Female
Enrollment 38 participants
Start Date 2024-04-25
Primary Completion 2026-11 (estimated)
Study Completion 2026-11 (estimated)
Updated on ClinicalTrials.gov 2026-06-03