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

NCT00184093 · ClinicalTrials.gov registry record · Phase 1

Study of Gemcitabine and Concurrent Radiation Followed by Adjuvant Hysterectomy in Bulky Stage Ib and IIa Cervical Carcinoma

A Phase 1 study, sponsored by University of Southern California.

Completed
Registry status
Phase 1
Development phase
35
Enrollment target

NCT00184093: Completed Phase 1 study, sponsored by University of Southern California.

NCT00184093 is a Phase 1 study that has completed, run by University of Southern California. The registered enrollment target is 35 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (42% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00184093, a Phase 1 study, has completed, sponsored by University of Southern California.

COMPLETED
Registry status
Phase 1
Development phase
35 participants
Enrollment target

Study Summary

The purpose of this study is first to establish what is the ideal dose of gemcitabine, a chemotherapy agent, when given in combination with radiation. In addition, the investigators want to determine the side effects and the effectiveness of this combination. The investigators will also study several markers to try to identify markers or tests that will predict which patients will benefit more from this treatment.

Primary Outcome

Summary of grade 3 or higher toxicities as per Common Toxicity Criteria version 2.0. Phase 1 and 2 Combined (N=35)

Interventions

  • DRUG Gemcitabine

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 1999-06
Est. Completion 2009-05
Phase Phase 1
University of Southern California

617 total trials

What the finished NCT00184093 record still lists

NCT00184093 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 35 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (42% lower).

The record links to 0 conditions, and to 1 intervention - of which Gemcitabine is the first listed.

NCT00184093 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00184093 about?

NCT00184093 is a clinical study titled "Study of Gemcitabine and Concurrent Radiation Followed by Adjuvant Hysterectomy in Bulky Stage Ib and IIa Cervical Carcinoma". The purpose of this study is first to establish what is the ideal dose of gemcitabine, a chemotherapy agent, when given in combination with radiation. In addition, the investigators want to determine the side effects and the effectiveness of this combination. The investigators will also study severa...

What is the current status of trial NCT00184093?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 35 participants. The study started on 1999-06. Estimated completion is 2009-05.

What interventions are being tested in trial NCT00184093?

The interventions under investigation include: Gemcitabine (DRUG).

Who is sponsoring clinical trial NCT00184093?

This trial is sponsored by University of Southern California, which has 617 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00184093's enrollment target sits among peer trials

35 1258th of 2000 higher than 728 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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

  • NCT01697371 · 35 participants · NA

    Proton Therapy in the Treatment of Liver Metastases

  • NCT01940757 · 35 participants · Phase 1

    Experimental Infection of Hookworm-naïve Adults With Dermally-applied Infectious Necator Americanus Hookworm Larvae

  • NCT02235857 · 35 participants · NA

    Post Approval Study of Liposorber LA-15 System for the Treatment of Focal Segmental Glomerulosclerosis in Children

  • NCT02637934 · 35 participants · Phase 1

    Phase I Pilot Study of Biodistribution, Metabolism and Excretion of Novel Radiotracer [18F]Fluorthanatrace (FTT) by PET/CT

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 NCT00184093, the US trial registry maintained by the National Library of Medicine. NCT00184093 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.