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NCT02251652 · ClinicalTrials.gov registry record · Phase 4

Safety and Efficacy of Ingenol Mebutate 0.05% Gel When Used After Cryotherapy in the Hypertrophic Actinic Keratoses

A Phase 4 study, sponsored by Icahn School of Medicine at Mount Sinai.

Completed
Registry status
Phase 4
Development phase
16
Enrollment target

NCT02251652 is a Phase 4 study that has completed, run by Icahn School of Medicine at Mount Sinai. The registered enrollment target is 16 participants.

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The verdict

NCT02251652, a Phase 4 study, has completed, sponsored by Icahn School of Medicine at Mount Sinai.

COMPLETED
Registry status
Phase 4
Development phase
16 participants
Enrollment target

Study Summary

Sequential therapy with cryosurgery and ingenol mebutate may optimize the treatment of hypertrophic AKs and also treat non-hypertrophic AKs in this anatomic location. Furthermore, use of ingenol mebutate will also be evaluated for potential treatment of subclinical lesions.

Interventions

  • PROCEDURE Cryotherapy
  • DRUG Ingenol Mebutate

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2013-04
Est. Completion 2015-08
Phase Phase 4

What the Registry Record Tells You About NCT02251652

The ClinicalTrials.gov registry entry for NCT02251652 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 16 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Icahn School of Medicine at Mount Sinai, which has 708 total studies on file at ClinicalTrials.gov.

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

NCT02251652 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02251652 about?

NCT02251652 is a clinical study titled "Safety and Efficacy of Ingenol Mebutate 0.05% Gel When Used After Cryotherapy in the Hypertrophic Actinic Keratoses". Sequential therapy with cryosurgery and ingenol mebutate may optimize the treatment of hypertrophic AKs and also treat non-hypertrophic AKs in this anatomic location. Furthermore, use of ingenol mebutate will also be evaluated for potential treatment of subclinical lesions.

What is the current status of trial NCT02251652?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 16 participants. The study started on 2013-04. Estimated completion is 2015-08.

What interventions are being tested in trial NCT02251652?

The interventions under investigation include: Cryotherapy (PROCEDURE), Ingenol Mebutate (DRUG).

Who is sponsoring clinical trial NCT02251652?

This trial is sponsored by Icahn School of Medicine at Mount Sinai, which has 708 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.