Full results & analysis
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
IV vs PO Acetaminophen for Pain in Oocyte Retrieval
NCT03073980Phase 4
Key facts
- Status
- Completed
- Start
- Sep 2019
- Primary completion
- Nov 2020
- Countries
- 1
- Sponsor
- Massachusetts General Hospital
- Modality
- Small Molecules
- Drugs
- acetaminophen
- Conditions
- postoperative pain
01
Overview
Phase 4, randomised, double-blind trial of acetaminophen in postoperative pain (3 arms), sponsored by Massachusetts General Hospital. Primary endpoints: Post-operative Pain Score Difference 10 Mins From Pre-operative at 10 months and Time to Discharge From the Post-operative Recovery Room. Started Sep 2019; status: completed.
02
Design
3 arms- Study design
- RandomizedDouble-blind
IV Acetaminophen
1000mg IV Acetaminophen + PO Placebo
PO Acetaminophen
1000mg PO Acetaminophen + IV Placebo
Placebo
IV Placebo + PO Placebo
03
Who it enrols
Adult females undergoing oocyte retrieval, excluding those with liver disease, renal impairment, chronic opiate use, or weight < 50kg.
04
Endpoints
Primary
Post-operative Pain Score Difference 10 Mins From Pre-operative
Time to Discharge From the Post-operative Recovery Room
Secondary
Procedure Length
Postoperative Nausea and Vomiting
Oocyte Yield
Rescue Medication Required
Beyond the preview
Go deeper on NCT03073980.
Full results, competitive context and analysis are in the Gosset platform.
Competitive context
Available in the Gosset platform where reported.
Bring the full picture into focus.
See how Gosset can support your research on NCT03073980.