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NCT05286307 · ClinicalTrials.gov registry record · Phase 4

Adductor Canal Block and IPACK Block vs. Isolated Adductor Canal Block for Post-Operative Analgesia Following ACL Reconstruction With Bone Patellar Tendon Bone Autograft:

A Phase 4 study, sponsored by NYU Langone Health.

Completed
Registry status
Phase 4
Development phase
102
Enrollment target

NCT05286307: Completed Phase 4 study, sponsored by NYU Langone Health.

NCT05286307 is a Phase 4 study that has completed, run by NYU Langone Health. The registered enrollment target is 102 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05286307, a Phase 4 study, has completed, sponsored by NYU Langone Health.

COMPLETED
Registry status
Phase 4
Development phase
102 participants
Enrollment target

Study Summary

A randomized, single-blind, single-center study measuring the effects of adductor canal block combined with IPACK infiltration compared to adductor canal block alone on post-operative pain and opioid consumption in patients undergoing ACL reconstruction with Bone Patellar Tendon Bone Autograft

Primary Outcome

Opioid utilization for the first 24 hours after surgery, including during surgery, is calculated as oral morphine equivalent.

Interventions

  • DRUG IPACK block

Trial Details

FieldValue
Enrollment Target 102 participants
Start Date 2022-07-11
Est. Completion 2023-12-18
Phase Phase 4
NYU Langone Health

1,164 total trials

What the finished NCT05286307 record still lists

NCT05286307 is an interventional study that assigns participants to a tested intervention. The registered 102 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (80% lower).

The record links to 0 conditions, and to 1 intervention - of which IPACK block is the first listed.

NCT05286307 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05286307 about?

NCT05286307 is a clinical study titled "Adductor Canal Block and IPACK Block vs. Isolated Adductor Canal Block for Post-Operative Analgesia Following ACL Reconstruction With Bone Patellar Tendon Bone Autograft:". A randomized, single-blind, single-center study measuring the effects of adductor canal block combined with IPACK infiltration compared to adductor canal block alone on post-operative pain and opioid consumption in patients undergoing ACL reconstruction with Bone Patellar Tendon Bone Autograft

What is the current status of trial NCT05286307?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 102 participants. The study started on 2022-07-11. Estimated completion is 2023-12-18.

What interventions are being tested in trial NCT05286307?

The interventions under investigation include: IPACK block (DRUG).

Who is sponsoring clinical trial NCT05286307?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05286307's enrollment target sits among peer trials

102 764th of 2000 higher than 1,235 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT05286307, the US trial registry maintained by the National Library of Medicine. NCT05286307 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.