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NCT06617949 · ClinicalTrials.gov registry record · Early Phase 1

Evaluating Pain Control Strategies in Postpartum Patients on Opioid Use Disorder Medications.

A Early Phase 1 study of Substance Use Disorder (SUD), sponsored by Medical College of Wisconsin.

Recruiting
Registry status
Early Phase 1
Development phase
20
Enrollment target
2
Study locations

NCT06617949: Recruiting Early Phase 1 study of Substance Use Disorder (SUD), sponsored by Medical College of Wisconsin.

NCT06617949 is a Early Phase 1 study of Substance Use Disorder (SUD) that is actively recruiting participants, run by Medical College of Wisconsin. The registered enrollment target is 20 participants, below the 248-participant average among 15 other Substance Use Disorder (SUD) trials with a reported enrollment target (92% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06617949, a Early Phase 1 study of Substance Use Disorder (SUD), is actively recruiting participants, sponsored by Medical College of Wisconsin.

RECRUITING
Registry status
Early Phase 1
Development phase
20 participants
Enrollment target
2
Study locations

Study Summary

The purpose of this study is to investigate the efficacy of three different modalities of post-operative pain control in parturient with opioid use disorders. The investigators aim to determine whether the different approach utilized show better outcomes with pain management and if there are any association with reduction of symptoms of anxiety, depression, and overall well-being.

Primary Outcome

Number of participants with significant change in pain assessment scores and any association with reduction of symptoms of anxiety, depression, and overall well-being.

Interventions

  • DRUG Regional Anesthesia
  • DRUG Hydromorphone Patient Controlled Analgelsic
  • PROCEDURE Epidural local anesthetic infusion

Study Locations (2)

Wisconsin

  • Froedtert Hospital Milwaukee, Wisconsin 53226 - Milwaukee
  • Froedtert Hospital - Milwaukee

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2025-01-16
Est. Completion 2028-12
Phase Early Phase 1
Medical College of Wisconsin

447 total trials

What NCT06617949 shows while recruiting

NCT06617949 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 248-participant average among 15 other Substance Use Disorder (SUD) trials with a reported enrollment target (92% lower).

The record links to 1 condition, with Substance Use Disorder (SUD) appearing as the primary indexed condition, and to 3 interventions - of which Regional Anesthesia is the first listed.

NCT06617949 reports a single indexed study location in Wisconsin.

Frequently Asked Questions

What is clinical trial NCT06617949 about?

NCT06617949 is a clinical study titled "Evaluating Pain Control Strategies in Postpartum Patients on Opioid Use Disorder Medications.". The purpose of this study is to investigate the efficacy of three different modalities of post-operative pain control in parturient with opioid use disorders. The investigators aim to determine whether the different approach utilized show better outcomes with pain management and if there are any ass...

What is the current status of trial NCT06617949?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 20 participants. The study started on 2025-01-16. Estimated completion is 2028-12.

What conditions does trial NCT06617949 study?

This clinical trial studies the following conditions: Substance Use Disorder (SUD).

What interventions are being tested in trial NCT06617949?

The interventions under investigation include: Regional Anesthesia (DRUG), Hydromorphone Patient Controlled Analgelsic (DRUG), Epidural local anesthetic infusion (PROCEDURE).

Who is sponsoring clinical trial NCT06617949?

This trial is sponsored by Medical College of Wisconsin, which has 447 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06617949 being conducted?

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

Similar trials for Substance Use Disorder (SUD)

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 NCT06617949's enrollment target sits among peer trials

20 15th of 15 higher than 1 of 15 other Substance Use Disorder (SUD) trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Substance Use Disorder (SUD) 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 NCT06617949, the US trial registry maintained by the National Library of Medicine. NCT06617949 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.