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

NCT00845754 · ClinicalTrials.gov registry record · NA

Post-Operative Treatment With Ketorolac After Abdominal Myomectomy

A NA study, sponsored by Ascher-Walsh, Charles, M.D..

Completed
Registry status
NA
Development phase
112
Enrollment target

NCT00845754: Completed NA study, sponsored by Ascher-Walsh, Charles, M.D..

NCT00845754 is a NA study that has completed, run by Ascher-Walsh, Charles, M.D.. The registered enrollment target is 112 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00845754, a NA study, has completed, sponsored by Ascher-Walsh, Charles, M.D..

COMPLETED
Registry status
NA
Development phase
112 participants
Enrollment target

Study Summary

The purpose of this study is to determine if ketorolac, given after abdominal myomectomy, will decrease the frequency of post-oerative fevers as well as improve post-operative pain management.

Interventions

  • DRUG saline
  • DRUG ketorolac

Trial Details

FieldValue
Enrollment Target 112 participants
Start Date 1999-09
Est. Completion 2001-08
Phase NA
Ascher-Walsh, Charles, M.D.

4 total trials

What the finished NCT00845754 record still lists

NCT00845754 is an interventional study that assigns participants to a tested intervention. The registered 112 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).

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

NCT00845754 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00845754 about?

NCT00845754 is a clinical study titled "Post-Operative Treatment With Ketorolac After Abdominal Myomectomy". The purpose of this study is to determine if ketorolac, given after abdominal myomectomy, will decrease the frequency of post-oerative fevers as well as improve post-operative pain management.

What is the current status of trial NCT00845754?

This trial is currently completed. It is a NA study. The enrollment target is 112 participants. The study started on 1999-09. Estimated completion is 2001-08.

What interventions are being tested in trial NCT00845754?

The interventions under investigation include: saline (DRUG), ketorolac (DRUG).

Who is sponsoring clinical trial NCT00845754?

This trial is sponsored by Ascher-Walsh, Charles, M.D., which has 4 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00845754's enrollment target sits among peer trials

112 813th of 2000 higher than 1,185 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

  • NCT04511013 · 112 participants · Phase 2

    A Study to Compare the Administration of Encorafenib + Binimetinib + Nivolumab Versus Ipilimumab + Nivolumab in BRAF-V600 Mutant Melanoma With Brain Metastases

  • NCT04551560 · 112 participants · NA

    Stress and Congestive Heart Failure

  • NCT04872166 · 112 participants · Phase 1

    A Study of BTX-A51 in People With Advanced Solid Tumor and Breast Cancer

  • NCT05024773 · 112 participants · Phase 3

    Study of ONCOFID-P-B (PACLITAXEL-HYALURONIC ACID)

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 NCT00845754, the US trial registry maintained by the National Library of Medicine. NCT00845754 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.