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Dermatop (Prednicarbate Topical) - Summary



DERMATOP® Ointment (prednicarbate ointment) 0.1% contains the non-halogenated prednisolone derivative prednicarbate. The topical corticosteroids constitute a class of primarily synthetic steroids used topically as anti-inflammatory and anti-pruritic agents. Each gram of DERMATOP Ointment 0.1% contains 1.0mg of prednicarbate in a base consisting of white petrolatum, octyldodecanol, glyceryl oleate, propylene glycol, citric acid, and propyl gallate.

DERMATOP Ointment 0.1% is a medium potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses.

See all Dermatop indications & dosage >>


Media Articles Related to Dermatop ( Topical)

FDA Approves 1st Topical Gel to Ease Redness of Rosacea
Source: MedicineNet brimonidine Specialty [2013.08.28]
Title: FDA Approves 1st Topical Gel to Ease Redness of Rosacea
Category: Health News
Created: 8/27/2013 12:35:00 PM
Last Editorial Review: 8/28/2013 12:00:00 AM

Burn Risk Seen with Topical Pain Relievers
Source: MedPage Today Product Alert [2012.09.13]
WASHINGTON -- The FDA warned Thursday of the risks of rare but serious chemical burns with certain over-the-counter topical pain relievers, including Bengay, Capzasin, Flexall, Icy Hot, and Mentholatum.

Clinical trial results of potential migraine therapy to be presented by Achelios Therapeutics
Source: Headache / Migraine News From Medical News Today [2015.04.21]
TOPOFEN (TM) is a new and novel topical medication for the treatment of acute migraineAchelios Therapeutics will announce results from a Phase IIa placebo-controlled clinical trial in moderate...

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Published Studies Related to Dermatop ( Topical)

Efficacy of Benzocaine 20% Topical Anesthetic Compared to Placebo Prior to Administration of Local Anesthesia in the Oral Cavity: A Randomized Controlled Trial. [2015]
The aim of the present study was to compare the effects of a topical anesthetic to a placebo on pain perception during administration of local anesthesia in 2 regions of the oral cavity. A split-mouth, double-blind, randomized clinical trial design was used...

Treatment of palmar-plantar erythrodysesthesia (PPE) with topical sildenafil: a pilot study. [2015]
treatment of PPE... CONCLUSIONS: In this limited, single-center study, topical cream containing 1 %

Topical analgesia treats pain and decreases propofol use during lumbar punctures in a randomized pediatric leukemia trial. [2015]
CONCLUSIONS: This study demonstrated that the combination of EMLA cream with

Effectiveness of topical curcumin for treatment of mastitis in breastfeeding women: a randomized, double-blind, placebo-controlled clinical trial. [2014]
inflammation in women suffering from lactational mastitis... CONCLUSION: The results of the current study indicate that topical preparation of

"Coffee plus honey" versus "topical steroid" in the treatment of chemotherapy-induced oral mucositis: a randomised controlled trial. [2014]
steroid, honey, honey plus coffee) in patients suffering from oral mucositis... CONCLUSION: Oral mucositis can be successfully treated by a combination of honey

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Clinical Trials Related to Dermatop ( Topical)

Standardized Time- and Score-oriented Treatment of Moderate and Severe Atopic Dermatitis [Completed]
The study was designed to test the hypothesis whether a standardized, time-and score-oriented treatment following a strict evidence based algorithm is equally effective to a standard treatment regimen for moderate to severe atopic dermatitis. Study Type: Mono-centre study, patients are blinded, physicians are randomized to either treat study- or controll group Eligible are patients age 2 years or older with SCORAD >= 20 Duration: 12 Months, study visits every 4 weeks. Primary endpoint is Difference between Baseline SCORAD and mean SCORAD under treatment. Secundary endpoints are quality of life, safety and economic burden in both treatment groups.

Bisphosphonate and Anastrozole Trial - Bone Maintenance Algorithm Assessment [Completed]
The purpose of this study is to evaluate the use of an oral bisphosphonate (alendronate) in preventing bone loss in postmenopausal women with early breast cancer who are receiving anastrozole therapy, and to determine how long alendronate treatment is needed.

Fexofenadine in Pruritic Skin Disease [Completed]

European Survey of Non-Variceal Upper Gastro Intestinal Bleeding (NVUGIB) [Completed]

Evaluation of Patient Characteristics and Treatment Approaches to Patients With Bipolar Disorder in Turkey [Completed]
A registry study to identify the patient-diagnosis-treatment characteristic profile of patients with bipolar disorder in Turkey.

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Page last updated: 2015-08-10

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