Double-blind, crossover, placebo-controlled clinical trial with clobetasol propionate in desquamative gingivitis

Double-blind, crossover, placebo-controlled clinical trial with clobetasol propionate in desquamative gingivitis

Ana Carolina Fragoso Motta^I,II; Carina Domaneschi^I; Marilena Chinali Komesu^II; Cacilda da Silva Souza^III; Valéria Aoki^IV; Dante Antonio Migliari^I

^IDepartment of Oral Diagnosis, Dental School, University of São Paulo, São Paulo, SP, Brazil

^IIDepartment of Morphology, Stomatology and Physiology, Ribeirão Preto Dental School, University of São Paulo, Ribeirão Preto, SP, Brazil

^IIIDepartment of Internal Medicine, Medical School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil

^IVDepartment of Dermatology, Medical School, University of São Paulo, São Paulo, SP, Brazil

^{Correspondence}

ABSTRACT

The aim of this study was to evaluate the efficacy of a 0.05% clobetasol propionate ointment administered in trays to 22 patients with desquamative gingivitis in a double-blind, crossover, placebo-controlled trial. Patients received container number 1 and were instructed to apply the ointment 3 times a day for 2 weeks, and to reduce the application to once a day in the third week. Next, the patients were then instructed to discontinue the treatment for 2 weeks, and were then given container 2, used in the same way and for the same length of time as container 1. Regarding signs, 17 patients presented some improvement, while 5 experienced worsening with clobetasol propionate. With the placebo, 14 patients presented some improvement, and 8 patients presented worsening. For symptoms, there was complete improvement in 2 patients, partial improvement in 12, no response in 7, and worsening in 1 with clobetasol propionate. With the placebo, there was partial improvement in 8 patients, no response in 12 and worsening in 2. No statistically significant difference was found between clobetasol and placebo (p>0.05). Within the period designed to treat the gingival lesions of the patients, clobetasol propionate did not significantly outperform the placebo.

Key Words: immunobullous disease, oral mucosa, clobetasol propionate.

RESUMO

O objetivo deste estudo foi avaliar a eficácia do propionato de clobetasol a 0,05% administrada com moldeiras em 22 pacientes com gengivite descamativa por meio de estudo duplo-cego, cruzado, placebo-controlado. Pacientes receberam bisnaga número 1 e foram instruídos a aplicar a pomada 3 vezes ao dia por um período de 2 semanas, e reduzir a aplicação para 1 vez ao dia na terceira semana. Os pacientes foram instruídos a suspender o tratamento por 2 semanas, e então receberam a bisnaga 2, usando-a da mesma maneira que o container 1. Com relação aos sinais, 17 pacientes apresentaram alguma melhora, enquanto 5 apresentaram piora com o propionato de clobetasol. Com o uso do placebo, 14 pacientes apresentaram alguma melhora, e 8 pacientes apresentaram piora do seu quadro clínico. Com relação aos sintomas, houve completa melhora em 2 pacientes, melhora parcial em 12, ausência de resposta em 7, e piora em 1 pacientes durante o uso do propionato de clobetasol. Com o uso do placebo, houve melhora parcial em 8 pacientes, ausência de resposta em 12 e piora dos sintomas em 2 pacientes. Não foi verificada diferença estatisticamente significante em nenhum dos parâmetros entre o uso do clobetasol e placebo; p>0,05. Baseado no protocolo utilizado neste grupo de pacientes, o propionato de clobetasol não demonstrou efetividade significante quando comparado ao placebo.

INTRODUCTION

Management of the gingival manifestations, clinically known as desquamative gingivitis, of autoimmune and inflammatory mucocutaneous diseases represents a great challenge to oral medicine clinicians, since most of these diseases are of a chronic nature (1-3). While systemic therapy may be required for the underlying disease, especially in cases associated with pemphigus vulgaris (PV), topical corticosteroids are often the mainstay for the treatment of localized gingival lesions (4-8). Clobetasol propionate has yielded good results with minimal side effects when properly used (5,9-11). Some studies have reported good outcomes for patients with oral lesions treated with clobetasol propionate in a mouthwash (3), and in an ointment with or without an adherent vehicle (7-12). However, it may be difficult to apply the corticosteroid to the entire lesional surface in patients with extensive gingival lesions. It has also been reported that the grainy texture of the paste with adherent vehicle is generally disliked, often affecting patient compliance. In addition, physiological mouth movements can displace the corticosteroid from its initial location, precluding good control of the contact time between the corticosteroid and the lesion (6,7,12). The use of a tray may provide a solution to this problem because it restrains the ointment and provides an occlusive contact between the corticosteroid and the lesions (12,13). The present double-blind, crossover, placebo-controlled study was carried out to evaluate the efficacy of clobetasol propionate administered in trays for the treatment of gingival manifestations of autoimmune and inflammatory mucocutaneous diseases.

MATERIAL AND METHODS

Patients

Twenty-two patients (17 women and 5 men; mean age = 50.6 ± 16.38 years; range 25-78 years) with chronic and symptomatic gingival lesions caused by autoimmune and inflammatory mucocutaneous diseases participated in the study. The patients were divided into 2 groups: group 1 consisted of 5 patients, all women, mean age 48.2 ± 8.13 years (range 38-58 years), treated systemically with prednisone and/or azathioprine for at least 6 months for control of their mucocutaneous diseases. All patients in this group presented PV; the duration of the disease was 8.2 ± 3.42 years (range 4-11 years). Group 2 consisted of 17 patients, 12 women, 5 men, mean age 51.4 ± 18.25 years (range 25-78 years), not under systemic treatment. In this group, 3 patients presented PV, 5 presented mucous membrane pemphigoid (MMP), and 9 had oral lichen planus (OLP); the duration of these diseases, taken together, was 5.6 ± 4.04 years, range 1-15 years. The characteristics of the patients are shown in Table 1.

The diagnosis of these diseases was made based on medical history and clinical examination, together with histopathologic (light microscopy - hematoxylin and eosin) and direct immunofluorescence findings of a biopsy specimen taken from the perilesional gingival mucosa. The clinical criteria for inclusion in this study were: presence of erythema, atrophy, vesicobullous areas, erosions, ulcerations and desquamative lesions, in multiple associations or not. Subjects were excluded if they presented disseminated mucocutaneous diseases or exacerbation of their diseases during the study period, or if they were taking any drugs capable of inducing lichenoid reactions. Blood pressure, glycemia, complete blood counts, and presence of candidosis were recorded at the start and at the end of the each protocol phase. Oral candidosis was diagnosed by evidence of fungal hyphae detected by exfoliative cytology of the gingival mucosa (direct exam with 10% KOH and periodic acid Schiff staining). The trial was approved by the local Research Ethics Committee and all subjects gave written informed consent to participate.

Drug

The drug under study was a 0.05% clobetasol propionate ointment (0.5 mg of clobetasol 17-propionate). The efficacy of this corticosteroid was compared to that of a placebo (hydroxylethyl cellulose) with the same physical characteristics as the corticosteroid (odorless, tasteless, and colorless). The ointments were prepared in equal containers of 30 g (containers number 1 and 2). The containers with randomization codes were obtained by Galderma Brasil Ltda, São Paulo, SP, Brazil. The code was not broken until completion of the crossover study.

Study Design

After an initial periodontal treatment, a topical application of ointments was instituted using trays of silicone rubber made on cast impressions. The patients received container number 1 and were instructed to apply the ointment with the tray for 20 min, 3 times daily (after breakfast, after lunch and after dinner), for 2 weeks. The frequency of use of ointment was reduced in the third week to once a day on alternate days. The patients were then instructed to discontinue the treatment for 2 weeks (washout period), and were given container number 2, to be used in the same way and at the same frequency and duration as container 1.

Clinical Response

Patients were examined before the trial and then at 2-week intervals throughout the trial. The patients' clinical evaluation was recorded at each visit on their charts, which consisted of a diagram of the gingival mucosa with 6 sites for tooth where the areas with lesions were marked. For signs, the response to therapy was defined as follows according to the percent of remission: complete (100%), excellent (75% to 99%), good (50% to 74%), poor (1% to 49%), no response, and worsened. Remission of symptoms was characterized as complete (no symptoms), partial, no response, and worsened. At every visit, the patients were also examined for the presence of side effects. Data were analyzed by Fisher's exact test. Significance was set at p<0.05.

RESULTS

Data on the clinical response of patients in each phase of this study are summarized in Tables 2 and 3. With respect to the evaluation of signs, 17 patients (77.2%) presented some improvement (Fig. 1), while 5 (22.7%) presented worsening with the use of clobetasol propionate. With the placebo, 14 patients (63.6%) presented some improvement, while 8 patients (36.4%) had worsening of signs (Table 2). For symptoms, complete improvement was observed in 2 patients (9.1%), partial improvement in 12 (54.5%), no response in 7 (31.8%) and worsening in 1 during the clobetasol phase. During the placebo phase, 8 patients (36.4%) had partial improvement, 12 (54.5%) no response and 2 (9.1%) showed worsening (Table 3).

Despite a tendency of the patients to respond slightly better to clobetasol in terms of improvement of signs and symptoms of their gingival lesions, no statistically significant difference was found between the results obtained with clobetasol propionate and the placebo (p>0.05). With respect to side effects, only 2 patients (9.1%) developed candidosis during the use of clobetasol propionate. These 2 patients were additionally treated with an antifungal (Nistatin) in oral suspension for 3 weeks, and a further retest for Candida sp was negative. No other side effects were observed in the patients of this study.

DISCUSSION

By comparing the severity of lesions at baseline with their outcome at the end of the trial, it was found that patients in the clobetasol phase showed a slightly better improvement of clinical signs and symptoms compared with those in the placebo phase, although the difference did not reach statistical significance (p>0.05). The failure of the corticosteroid to significantly outperform the placebo indicates that its vasoconstrictive, anti-inflammatory and immunosuppressive properties are not sufficient to suppress the immunologic and inflammatory mechanism involved in the development of the studied lesions. That both clobetasol propionate and the placebo ointment proved to be effective to some degree could be due to a protective and lubricating function of the ointment in conjunction with the use of trays. The occlusion produced by use of trays can have favored the protection of gingival tissues against functional movements of mouth.

Some double-blind studies showed the safety of topical clobetasol propionate in the treatment of oral vesiculo-erosive lesions (5,6,9,10,14). Clobetasol in orabase paste administered in trays 3 times daily around 2 weeks of treatment provided good outcomes in patients with severe erosive gingival lesions (11-13). On the other hand, clobetasol ointment used for 4 weeks in DG treatment had previously been found to be significantly less effective when it was compared with other drugs, such as tacrolimus (15).

It has been recognized that either systemic or topical corticotherapy may bring about serious side effects, such as increased susceptibility to infections, hypertension, hyperglycemia, fluid retention, and adrenal cortex suppression (1,6,16,17). With regard to topical therapy, the risk of side effects is increased when a high-potency corticosteroid is used in combination with occlusive techniques (17). Although only one study (3) has reported significant side effects with the use of topical high-potency corticosteroids in ulcerative and/or erosive oral lesions, there is a consensus among authors that patients under this type of treatment should be monitored carefully (12,16,17). The patients applied the corticosteroid to their gingival lesions for a period of 3 weeks. This length of time was sufficient to evaluate side effects, since some studies have indicated that adrenal suppression may occur as early as 24 h after initiating topical corticotherapy when used on the skin (16,18,19). The most common side effect of topical corticotherapy is candidosis (17,20). In the present study, only 2 patients (11.8%) developed candidosis after the use of clobetasol propionate. These patients were treated with a topical antifungal agent without interrupting the use of clobetasol. No other side effect was observed in the patients under study.

Topical corticosteroids, used as described in this paper, are usually safe and can be of some efficacy as adjunct therapy in combination with systemic treatment in patients with oral and skin lesions, or in the treatment of patients with gingival lesions alone. Although some of our patients did not show improvement of their gingival lesions while using clobetasol propionate, this may have been due to the limited sample size and the relatively short period of treatment. However, this shorter period does reduce the risk of side effects. A risk/benefit analysis should be undertaken when considering an increase in the dosage of any medication.

ACKNOWLEDGEMENTS

The Dr. Ana Carolina F. Motta was supported by a scholarship from the Coordination for the Improvement of Graduated Personnel. The authors acknowledge the support of Galderma Brazil Ltda. for the production of the ointments and randomization.

Accepted August 11, 2009

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Publication Dates

• Publication in this collection
  21 Sept 2009
• Date of issue
  2009