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NCT04003987 · ClinicalTrials.gov registry record · Phase 3
ESP Block VS TAP in Laparoscopic Hysterectomy
A Phase 3 study, sponsored by Indiana University.
- Completed
- Registry status
- Phase 3
- Development phase
- 78
- Enrollment target
NCT04003987 is a Phase 3 study that has completed, run by Indiana University. The registered enrollment target is 78 participants.
The verdict
NCT04003987, a Phase 3 study, has completed, sponsored by Indiana University.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 78 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the difference between two different pain control methods in patients who will be having a hysterectomy surgery. By collecting this data, we aim to show improved postoperative pain scores, decreased opioid needs, and decreased opioid side effects (nausea, sedation, ileus, urinary retention, respiratory depression).
Interventions
- DRUG Liposomal bupivacaine
- DRUG bupivacaine, 0.125%
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 78 participants |
| Start Date | 2019-05-01 |
| Est. Completion | 2021-03-04 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04003987
The ClinicalTrials.gov registry entry for NCT04003987 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 78 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Indiana University, which has 890 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Liposomal bupivacaine is the first listed.
NCT04003987 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04003987 about?
NCT04003987 is a clinical study titled "ESP Block VS TAP in Laparoscopic Hysterectomy". The purpose of this study is to compare the difference between two different pain control methods in patients who will be having a hysterectomy surgery. By collecting this data, we aim to show improved postoperative pain scores, decreased opioid needs, and decreased opioid side effects (nausea, seda...
What is the current status of trial NCT04003987?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 78 participants. The study started on 2019-05-01. Estimated completion is 2021-03-04.
What interventions are being tested in trial NCT04003987?
The interventions under investigation include: Liposomal bupivacaine (DRUG), bupivacaine, 0.125% (DRUG).
Who is sponsoring clinical trial NCT04003987?
This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.
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