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Seborrheic Keratosis clinical trials

View clinical trials related to Seborrheic Keratosis.

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NCT ID: NCT06046144 Completed - Melanoma Clinical Trials

Comparison of 3 in Vivo Microscopic Imaging Techniques for the Diagnosis of Pigmented Tumors

Micro3
Start date: November 2, 2022
Phase:
Study type: Observational

Reflectance confocal microscopy (RCM) is the reference in vivo imaging technique for identifying malignant melanocytic tumors prior to surgical excision. However, it is not widely used due to its high cost and highly technical and time-consuming nature. In addition to RCM, we currently use 2 less expensive dermatoscopes that also allow in vivo diagnosis: super-high magnification dermoscopy (D400) and Fluorescence-Advanced videodermatoscopy (FAV).

NCT ID: NCT05353374 Completed - Clinical trials for Seborrheic Keratosis

Effectiveness of Sodium Fusidate Ointment Compared to Petrolatum for Wound Healing Following Cauterization

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

A double-blind within person randomized controlled trial study was conducted on 90 wounds in 22 subjects. All wounds were randomized to receive either sodium fusidate ointment or petrolatum following cauterization.

NCT ID: NCT03846531 Completed - Clinical trials for Seborrheic Keratosis

Nano-Pulse Stimulation (NPS) in Seborrheic Keratosis Study

Start date: May 4, 2017
Phase: N/A
Study type: Interventional

The primary purpose of this trial is to evaluate Nano-Pulse Stimulation (NPS) to clear or remove Seborrheic Keratosis (SK) lesions from off-facial areas of healthy adult subjects.

NCT ID: NCT03487588 Completed - Clinical trials for Seborrheic Keratosis

An A Study Assessing Subject Satisfaction With A-101 Topical Solution for Seborrheic Keratoses

SK-FAN
Start date: March 21, 2018
Phase: Phase 4
Study type: Interventional

This study is an open-label study designed to evaluate subject's satisfaction after treatment of seborrheic keratoses with A-101 40%.

NCT ID: NCT03148691 Completed - Clinical trials for Seborrheic Keratosis

A Randomized, Vehicle-Controlled Study of 2 Concentrations of A-101 for the Treatment of Seborrheic Keratosis

Start date: May 17, 2017
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the safety and effectiveness of 2 concentrations of A-101 compared to Vehicle for the treatment of 4 seborrheic keratosis (SK) Target Lesions on the trunk, extremities and face.

NCT ID: NCT02667288 Completed - Clinical trials for Seborrheic Keratosis

An Open-Label Safety Study of A-101 Solution

Start date: January 2016
Phase: Phase 3
Study type: Interventional

This is an open-label safety study. During this study, the investigator will identify 4 eligible SK Target Lesions on each subject on the trunk, extremities and face.

NCT ID: NCT02667275 Completed - Clinical trials for Seborrheic Keratosis

A Randomized, Double-Blind, Vehicle-Controlled Study in Subjects With Seborrheic Keratosis

SK
Start date: January 2016
Phase: Phase 3
Study type: Interventional

This is a randomized, double-blind, vehicle-controlled, parallel group study.

NCT ID: NCT02667236 Completed - Clinical trials for Seborrheic Keratosis

A Study of A-101 Solution 40% in Subjects With Seborrheic Keratosis.

Start date: January 2016
Phase: Phase 3
Study type: Interventional

This is a randomized, double-blind, vehicle-controlled, parallel group study of A-101 Solution 40% compared with Vehicle Solution.

NCT ID: NCT02260180 Completed - Clinical trials for Seborrheic Keratosis

Study of A-101 for the Treatment of Seborrheic Keratosis

Start date: October 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and dose-response of 2 concentrations of A-101 versus a vehicle control in the treatment of seborrheic keratosis.

NCT ID: NCT02160626 Completed - Clinical trials for Seborrheic Keratosis

Dose-Response Profile of A-101 in Subjects With Seborrheic Keratosis

Start date: June 2014
Phase: Phase 2
Study type: Interventional

The main objective of this study is to evaluate the dose-response relationship of two concentrations of A-101 solution when applied to individual seborrheic keratosis (SK) lesions (target lesions) compared with a matching A-101 Solution Vehicle.