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NCT03188432 · ClinicalTrials.gov registry record · Phase 2

Hyperthermic Intraperitoneal Chemotherapy Trial Comparing Quality of Life in Patients With Stage IIIC-IV Ovarian, Fallopian Tube, or Primary Peritoneal Cancer

A Phase 2 study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
Phase 2
Development phase
50
Enrollment target

NCT03188432: Completed Phase 2 study, sponsored by Wake Forest University Health Sciences.

NCT03188432 is a Phase 2 study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 50 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (62% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03188432, a Phase 2 study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
Phase 2
Development phase
50 participants
Enrollment target

Study Summary

This phase II trial studies how well hyperthermic intraperitoneal chemotherapy works in improving quality of life in patients with stage IIIC-IV ovarian, fallopian tube, or primary peritoneal cancer. In hyperthermic intraperitoneal chemotherapy, the chemotherapy is warmed before being used and may help the drugs get into the cancer cells better, minimize the toxicity of the drugs on normal cells, and help to kill any cancer cells left over after surgery.

Primary Outcome

This is a descriptive study. QOL will be measured using the Fact-O questionnaire and treated as a continuous outcome. The distribution of QOL at 6 weeks post-treatment will be examined. Descriptive statistics such as mean, standard deviation, median and interquartile range will be calculated. The FACT-O consists of 39 questions answered with five-point Likert Scales (0-4). The possible range of scores is 0-156, and higher scores indicate a better quality of life.

Interventions

  • DRUG Carboplatin
  • OTHER Quality-of-Life Assessment
  • OTHER Questionnaire Administration
  • PROCEDURE Cytoreductive Surgery

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2019-01-02
Est. Completion 2024-02-08
Phase Phase 2
Wake Forest University Health Sciences

1,140 total trials

What the finished NCT03188432 record still lists

NCT03188432 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (62% lower).

The record links to 0 conditions, and to 4 interventions - of which Carboplatin is the first listed.

NCT03188432 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03188432 about?

NCT03188432 is a clinical study titled "Hyperthermic Intraperitoneal Chemotherapy Trial Comparing Quality of Life in Patients With Stage IIIC-IV Ovarian, Fallopian Tube, or Primary Peritoneal Cancer". This phase II trial studies how well hyperthermic intraperitoneal chemotherapy works in improving quality of life in patients with stage IIIC-IV ovarian, fallopian tube, or primary peritoneal cancer. In hyperthermic intraperitoneal chemotherapy, the chemotherapy is warmed before being used and may h...

What is the current status of trial NCT03188432?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 50 participants. The study started on 2019-01-02. Estimated completion is 2024-02-08.

What interventions are being tested in trial NCT03188432?

The interventions under investigation include: Carboplatin (DRUG), Quality-of-Life Assessment (OTHER), Questionnaire Administration (OTHER), Cytoreductive Surgery (PROCEDURE).

Who is sponsoring clinical trial NCT03188432?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03188432's enrollment target sits among peer trials

50 1195th of 2000 higher than 740 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

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Source: ClinicalTrials.gov NCT03188432, the US trial registry maintained by the National Library of Medicine. NCT03188432 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.