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NCT06593665 · ClinicalTrials.gov registry record · Phase 3

Intrathecal Morphine Versus Intravenous Methadone for Postoperative Analgesia Following Retroperitoneal Lymph Node Dissection.

A Phase 3 study of Testicular Cancer, sponsored by Indiana University.

Recruiting
Registry status
Phase 3
Development phase
142
Enrollment target
2
Study locations

NCT06593665: Recruiting Phase 3 study of Testicular Cancer, sponsored by Indiana University.

NCT06593665 is a Phase 3 study of Testicular Cancer that is actively recruiting participants, run by Indiana University. The registered enrollment target is 142 participants, above the 82-participant average among 11 other Testicular Cancer trials with a reported enrollment target (73% higher). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06593665, a Phase 3 study of Testicular Cancer, is actively recruiting participants, sponsored by Indiana University.

RECRUITING
Registry status
Phase 3
Development phase
142 participants
Enrollment target
2
Study locations

Study Summary

This randomization study is to compare both intrathecal morphine and intravenous methadone, which are both standard of care, for pain management in patients undergoing retroperitoneal lymph node dissections for primary testicular cancer. Investigators plan to compare their analgesic effectiveness at different postoperative time intervals.

Primary Outcome

Cumulative Milligrams of morphine equivalent (MME) consumption

Conditions Studied

Interventions

  • DRUG Inrathecal Morphine
  • DRUG Intravenous Methadone

Study Locations (2)

Indiana

  • Indiana Univeristy - Indianapolis
  • Indiana University Hospital - Indianapolis

Trial Details

FieldValue
Enrollment Target 142 participants
Start Date 2024-09-10
Est. Completion 2026-12-31
Phase Phase 3
Indiana University

890 total trials

What NCT06593665 shows while recruiting

NCT06593665 is an interventional study that assigns participants to a tested intervention. The registered 142 participants enrollment target is mid-sized for trials with a published cap, above the 82-participant average among 11 other Testicular Cancer trials with a reported enrollment target (73% higher).

The record links to 1 condition, with Testicular Cancer appearing as the primary indexed condition, and to 2 interventions - of which Inrathecal Morphine is the first listed.

NCT06593665 reports a single indexed study location in Indiana.

Frequently Asked Questions

What is clinical trial NCT06593665 about?

NCT06593665 is a clinical study titled "Intrathecal Morphine Versus Intravenous Methadone for Postoperative Analgesia Following Retroperitoneal Lymph Node Dissection.". This randomization study is to compare both intrathecal morphine and intravenous methadone, which are both standard of care, for pain management in patients undergoing retroperitoneal lymph node dissections for primary testicular cancer. Investigators plan to compare their analgesic effectiveness at...

What is the current status of trial NCT06593665?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 142 participants. The study started on 2024-09-10. Estimated completion is 2026-12-31.

What conditions does trial NCT06593665 study?

This clinical trial studies the following conditions: Testicular Cancer.

What interventions are being tested in trial NCT06593665?

The interventions under investigation include: Inrathecal Morphine (DRUG), Intravenous Methadone (DRUG).

Who is sponsoring clinical trial NCT06593665?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06593665 being conducted?

This trial has 2 study locations across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Testicular Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06593665's enrollment target sits among peer trials

142 3rd of 11 higher than 9 of 11 other Testicular Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Testicular Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06593665, the US trial registry maintained by the National Library of Medicine. NCT06593665 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.