At a glance
ClinicalIndex Comparison RecordPhase 4Unknown· 100 enrolled
Drug / intervention
Fentanyl +2 moredrug
Likely dose
Fentanyl 1 mcg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Predictors of Postoperative Pain Following Oocyte Retrieval for Assisted Reproduction
In Brief
A Phase 4 clinical trial evaluating Fentanyl, Acetaminophen, and 1 other intervention for Oocyte Retrieval and Postoperative Pain. Targeting 100 participants across 1 site.
Detailed Summary
The central objective of this study will be to evaluate the relationship between estrogen levels and the pain following oocyte retrieval in women undergoing in vitro fertilization.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsOocyte Retrieval, Postoperative Pain
CountriesUnited States
Collaborators--
Timeline
Phase 4UnknownOverdue
2011201220132014201520162017201820192020202120222023202420252026
Enrollment StartMar 2011
First PostedApr 2017
Primary CompletionJun 2023
TodayJul 2026
First PostedApr 10, 2017
Enrollment StartMar 1, 2011
Primary CompletionJun 30, 2023
TodayJul 2, 2026
Enrollment to primary: 12.3 yearsPosted 9.2 years ago
Interventions
Fentanyldrug
0.5, 1 mcg/kg
Acetaminophendrug
Single + Oxycodone
Oxycodonedrug
With Acetaminophen