clindamycin-phosphate and Chronic-Disease

clindamycin-phosphate has been researched along with Chronic-Disease* in 2 studies

Reviews

1 review(s) available for clindamycin-phosphate and Chronic-Disease

ArticleYear
When do efficacy outcomes in clinical trials correlate with clinical relevance? analysis of clindamycin phosphate 1.2%-benzoyl peroxide 3.75% gel in moderate to severe acne vulgaris.
    Cutis, 2016, Volume: 98, Issue:1

    Acne vulgaris (AV) is a common skin disease that is challenging to successfully treat due to its complex underlying pathophysiology and chronicity. Unrealistic expectations based on the desire for rapid and complete clearance or local tolerability reactions related to topical medications often lead to incomplete adherence with therapy, premature treatment cessation, and poor therapeutic outcomes. Despite stressing to patients the importance of compliance and the lag time of several weeks before visible improvement may be noted with treatments for AV, data on evaluation of the time taken to achieve a clinically meaningful improvement of AV that may be perceived by clinicians and patients are limited. Clindamycin phosphate 1.2%-benzoyl peroxide 3.75% (clindamycin-BP 3.75%) gel has been shown in pivotal trials to be effective and well tolerated in patients with moderate to severe AV. This article reviews a new concept referred to as time to onset of action (TOA), which is described in detail and illustrated using the pivotal trial data with clindamycin-BP 3.75% gel for treatment of AV.

    Topics: Acne Vulgaris; Benzoyl Peroxide; Chronic Disease; Clindamycin; Clinical Trials as Topic; Dermatologic Agents; Humans; Patient Compliance; Treatment Outcome

2016

Other Studies

1 other study(ies) available for clindamycin-phosphate and Chronic-Disease

ArticleYear
Intraosseous injection of clindamycin phosphate into the chronic apical lesion of lower molar--a case report.
    Bosnian journal of basic medical sciences, 2005, Volume: 5, Issue:2

    Periapical disease is the result of bacteria, their product, and the host response to them. Early histological studies of diseased periapical tissue have not been able to demonstrate viable bacteria in the lesions studied. Recent reports indicate that many of periapical lesions are indeed infected before and after endodontic treatment. The validity and applicability of the microbial delivery overcome many disadvantages that we see with systemic drugs. In this case report we presented a novel approach of managing chronic diffuse periapical lesion of lower molar based on specific selection of intracanal medicament in combination with direct periapical injection. We used bacterial culturing and antibiotic sensitivity test to select specific intracanal medicament, in addition we presented an intraosseous injection technique to locally deliver the selected medicament directly into the periapical lesion. Our findings are encouraging and promising. The validity and applicability of the technique needs to be tested in a well controlled clinical trial.

    Topics: Adult; Anti-Bacterial Agents; Chronic Disease; Clindamycin; Female; Follow-Up Studies; Humans; Injections; Molar; Periapical Diseases; Treatment Outcome

2005