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NCT07221617 · ClinicalTrials.gov registry record · Phase 4
Oral Methadone in Cardiac Surgery
A Phase 4 study of Pain, Postoperative and Anesthesia, sponsored by Mayo Clinic.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT07221617 is a Phase 4 study of Pain, Postoperative and Anesthesia that is actively recruiting participants, run by Mayo Clinic. The registered enrollment target is 100 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (63% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07221617, a Phase 4 study of Pain, Postoperative and Anesthesia, is actively recruiting participants, sponsored by Mayo Clinic.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to compare the effects of administration of oral methadone preoperatively and intravenous methadone upon induction of general anesthesia on postoperative pain for patients undergoing elective cardiac surgery.
Conditions Studied
Interventions
- DRUG Methadone, oral
- DRUG Methadone, intravenously
Study Locations (1)
Minnesota
- Mayo Clinic in Rochester - Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2026-01-13 |
| Est. Completion | 2026-08 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07221617
The ClinicalTrials.gov registry entry for NCT07221617 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (63% lower). The listed sponsor is Mayo Clinic, which has 2,844 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 2 interventions - of which Methadone, oral is the first listed.
NCT07221617 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.
Frequently Asked Questions
What is clinical trial NCT07221617 about?
NCT07221617 is a clinical study titled "Oral Methadone in Cardiac Surgery". The purpose of this study is to compare the effects of administration of oral methadone preoperatively and intravenous methadone upon induction of general anesthesia on postoperative pain for patients undergoing elective cardiac surgery.
What is the current status of trial NCT07221617?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2026-01-13. Estimated completion is 2026-08.
What conditions does trial NCT07221617 study?
This clinical trial studies the following conditions: Pain, Postoperative, Anesthesia, Cardiac Surgery.
What interventions are being tested in trial NCT07221617?
The interventions under investigation include: Methadone, oral (DRUG), Methadone, intravenously (DRUG).
Who is sponsoring clinical trial NCT07221617?
This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07221617 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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