Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06532708 · ClinicalTrials.gov registry record · NA

Opioid Prescribing Practices in Laparoscopic Gynecologic Surgery

A NA study of Postoperative Pain and Opioid Use, sponsored by University of Tennessee.

Recruiting
Registry status
NA
Development phase
12
Enrollment target
1
Study location

NCT06532708: Recruiting NA study of Postoperative Pain and Opioid Use, sponsored by University of Tennessee.

NCT06532708 is a NA study of Postoperative Pain and Opioid Use that is actively recruiting participants, run by University of Tennessee. The registered enrollment target is 12 participants, below the 232-participant average among 120 other Postoperative Pain trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06532708, a NA study of Postoperative Pain and Opioid Use, is actively recruiting participants, sponsored by University of Tennessee.

RECRUITING
Registry status
NA
Development phase
12 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to compare opioid prescribing practices by either routine provider prescribing practices, or with the use of a calculator, i.e., the Opioid Calculator, published by the University of Michigan (www.opioidcalculator.org), with the intent of decreasing the number of pills.

Interventions

  • OTHER 5x Oxycodone Oral Tablets
  • OTHER 16x Oxycodone Oral Tablets

Study Locations (1)

Tennessee

  • University of Tennessee Health Science Center - Memphis

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2024-07-12
Est. Completion 2024-10-31
Phase NA
University of Tennessee

96 total trials

What NCT06532708 shows while recruiting

NCT06532708 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 232-participant average among 120 other Postoperative Pain trials with a reported enrollment target (95% lower).

The record links to 2 conditions, with Postoperative Pain appearing as the primary indexed condition, and to 2 interventions - of which 5x Oxycodone Oral Tablets is the first listed.

NCT06532708 reports a single indexed study location in Tennessee.

Frequently Asked Questions

What is clinical trial NCT06532708 about?

NCT06532708 is a clinical study titled "Opioid Prescribing Practices in Laparoscopic Gynecologic Surgery". The purpose of this study is to compare opioid prescribing practices by either routine provider prescribing practices, or with the use of a calculator, i.e., the Opioid Calculator, published by the University of Michigan (www.opioidcalculator.org), with the intent of decreasing the number of pills.

What is the current status of trial NCT06532708?

This trial is currently recruiting. It is a NA study. The enrollment target is 12 participants. The study started on 2024-07-12. Estimated completion is 2024-10-31.

What conditions does trial NCT06532708 study?

This clinical trial studies the following conditions: Postoperative Pain, Opioid Use.

What interventions are being tested in trial NCT06532708?

The interventions under investigation include: 5x Oxycodone Oral Tablets (OTHER), 16x Oxycodone Oral Tablets (OTHER).

Who is sponsoring clinical trial NCT06532708?

This trial is sponsored by University of Tennessee, which has 96 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06532708 being conducted?

This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Postoperative Pain

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 NCT06532708's enrollment target sits among peer trials

12 119th of 120 higher than 2 of 120 other Postoperative Pain trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Postoperative Pain 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02602769 · 12 participants

    Whole Transcriptome Profiling and Metabolic Phenotyping in Children With ROHHAD Syndrome

  • NCT02605421 · 12 participants · Phase 2

    Myeloablative Consolidation Therapy and Tandem Autologous Stem Cell Rescue in Patients With High-Risk Neuroblastoma

  • NCT02619448 · 12 participants · Early Phase 1

    Concurrent Chemotherapy Plus HFR Radiation Therapy in Inoperable NSCLC

  • NCT03311503 · 12 participants · Phase 1

    Phase I/II Trial of Lentiviral Gene Transfer for SCID-X1 With Low Dose Targeted Busulfan Conditioning

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06532708, the US trial registry maintained by the National Library of Medicine. NCT06532708 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.