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

NCT02840162 · ClinicalTrials.gov registry record · Phase 2

Pre-Prostatectomy Celecoxib or Placebo

A Phase 2 study, sponsored by OHSU Knight Cancer Institute.

Terminated
Registry status
Phase 2
Development phase
34
Enrollment target

NCT02840162: Clinical Trial Phase 2 study, sponsored by OHSU Knight Cancer Institute.

NCT02840162 is a Phase 2 study that was terminated before completion, run by OHSU Knight Cancer Institute. The registered enrollment target is 34 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (74% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02840162, a Phase 2 study, was terminated before completion, sponsored by OHSU Knight Cancer Institute.

TERMINATED
Registry status
Phase 2
Development phase
34 participants
Enrollment target

Study Summary

This study will seek to determine if the downstream effects of cyclooxygenase-2 (COX-2) inhibition suggested by preclinical systems occur in human prostate cancer. To answer this question, men who have chosen prostatectomy will be randomly assigned to preoperative treatment with celecoxib or placebo for four weeks. Carefully collected tumor, premalignant, and benign prostate tissue will then be examined for apoptosis, androgen receptor and prostaglandin E2 levels. Tumor COX-2 expression will be correlated with observed treatment effects. The data generated by this study will serve as a foundation for the development of COX-2 targeted therapies for prostate cancer, will provide preliminary evidence for larger scale clinical trials aimed at treatment and prevention of prostate cancer, and will validate current preclinical models used to study COX-2 in prostate cancer.

Primary Outcome

Percent positively staining cells with a minimum of 1000 total cells counted. Descriptive statistics will be conducted. The apoptotic index will be reported with 95% confidence intervals.

Interventions

  • DRUG Placebo
  • DRUG Celecoxib

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2001-05
Est. Completion 2011-05
Phase Phase 2
OHSU Knight Cancer Institute

211 total trials

Why NCT02840162 stopped before completion

NCT02840162 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 34 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (74% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02840162 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02840162 about?

NCT02840162 is a clinical study titled "Pre-Prostatectomy Celecoxib or Placebo". This study will seek to determine if the downstream effects of cyclooxygenase-2 (COX-2) inhibition suggested by preclinical systems occur in human prostate cancer. To answer this question, men who have chosen prostatectomy will be randomly assigned to preoperative treatment with celecoxib or placebo...

What is the current status of trial NCT02840162?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 34 participants. The study started on 2001-05. Estimated completion is 2011-05.

What interventions are being tested in trial NCT02840162?

The interventions under investigation include: Placebo (DRUG), Celecoxib (DRUG).

Who is sponsoring clinical trial NCT02840162?

This trial is sponsored by OHSU Knight Cancer Institute, which has 211 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02840162's enrollment target sits among peer trials

34 1539th of 2000 higher than 448 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

  • NCT02897063 · 34 participants · Phase 1

    Effects of Midodrine and Droxidopa on Splanchnic Capacitance in Autonomic Failure

  • NCT03906617 · 34 participants · Phase 4

    Bupivacaine/Epinephrine +Dexamethasone vs. Liposomal Bupivacaine

  • NCT03992378 · 34 participants · NA

    Neuromodulation to Regulate Inflammation and Autonomic Imbalance in Sepsis

  • NCT04047849 · 34 participants · Phase 4

    Latency Antibiotics in Previable PPROM, 18 0/7- 22 6/7 WGA

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02840162, the US trial registry maintained by the National Library of Medicine. NCT02840162 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.