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NCT03073980 · ClinicalTrials.gov registry record · Phase 4
Assessing Efficacy of Intravenous Acetaminophen for Perioperative Pain Control for Oocyte Retrieval
A Phase 4 study of Pain, Postoperative and Infertility, Female, sponsored by Massachusetts General Hospital.
- Completed
- Registry status
- Phase 4
- Development phase
- 161
- Enrollment target
- 1
- Study location
NCT03073980 is a Phase 4 study of Pain, Postoperative and Infertility, Female that has completed, run by Massachusetts General Hospital. The registered enrollment target is 161 participants, below the 271-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (41% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03073980, a Phase 4 study of Pain, Postoperative and Infertility, Female, has completed, sponsored by Massachusetts General Hospital.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 161 participants
- Enrollment target
- 1
- Study location
Study Summary
In this research study we want to learn more about how effective certain medications are at reducing pain after oocyte (egg) retrieval surgery and how effective they are at reducing the time between the retrieval and discharge from the hospital. We will compare three types of pre-operative medications: intravenous (IV) acetaminophen, oral (PO) acetaminophen, and placebo (no medication), which is the current typical care.
Conditions Studied
Interventions
- DRUG IV Acetaminophen
- DRUG PO Acetaminophen
- OTHER Placebo IV Acetaminophen
- OTHER Placebo PO Acetaminophen
Study Locations (1)
Massachusetts
- Massachusetts General Hospital - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 161 participants |
| Start Date | 2019-09-01 |
| Est. Completion | 2020-12-01 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03073980
The ClinicalTrials.gov registry entry for NCT03073980 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 161 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 271-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (41% lower). The listed sponsor is Massachusetts General Hospital, which has 2,032 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 4 interventions - of which IV Acetaminophen is the first listed.
NCT03073980 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.
Frequently Asked Questions
What is clinical trial NCT03073980 about?
NCT03073980 is a clinical study titled "Assessing Efficacy of Intravenous Acetaminophen for Perioperative Pain Control for Oocyte Retrieval". In this research study we want to learn more about how effective certain medications are at reducing pain after oocyte (egg) retrieval surgery and how effective they are at reducing the time between the retrieval and discharge from the hospital. We will compare three types of pre-operative medicatio...
What is the current status of trial NCT03073980?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 161 participants. The study started on 2019-09-01. Estimated completion is 2020-12-01.
What conditions does trial NCT03073980 study?
This clinical trial studies the following conditions: Pain, Postoperative, Infertility, Female.
What interventions are being tested in trial NCT03073980?
The interventions under investigation include: IV Acetaminophen (DRUG), PO Acetaminophen (DRUG), Placebo IV Acetaminophen (OTHER), Placebo PO Acetaminophen (OTHER).
Who is sponsoring clinical trial NCT03073980?
This trial is sponsored by Massachusetts General Hospital, which has 2,032 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03073980 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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