# An Efficacy and Safety Study to Compare Fentanyl Ionsys and Routine Care With Intravenous (IV) Morphine Patient-controlled Analgesia (PCA) in Participants Who Have Undergone Elective Major Abdominal or Orthopedic Surgery

> **NCT00766506** · PHASE4 · TERMINATED · sponsor: **Janssen-Cilag Ltd.** · enrollment: 108 (actual)

## Conditions studied

- Pain, Postoperative

## Interventions

- **DEVICE:** Fentanyl IONSYS
- **DEVICE:** Morphine IV PCA

## Key facts

- **NCT ID:** NCT00766506
- **Lead sponsor:** Janssen-Cilag Ltd.
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2008-05
- **Primary completion:** 2008-09
- **Final completion:** 2008-09
- **Target enrollment:** 108 (ACTUAL)
- **Why stopped:** Product class one recall
- **Last updated:** 2013-04-25


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00766506

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00766506, "An Efficacy and Safety Study to Compare Fentanyl Ionsys and Routine Care With Intravenous (IV) Morphine Patient-controlled Analgesia (PCA) in Participants Who Have Undergone Elective Major Abdominal or Orthopedic Surgery". Retrieved via AI Analytics 2026-06-14 from https://api.ai-analytics.org/clinical/NCT00766506. Licensed CC0.

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