跳至主要内容
临床试验/NCT07806357
NCT07806357已完成1 期

Efficacy and Safety of Prednisolone Monotherapy Versus Prednisolone Plus Methotrexate in Erythema Nodosum Leprosum (Type 2 Lepra Reaction)

Chittagong Medical College1 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2018年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
19
试验地点
1
主要终点
Efficacy and Safety of Prednisolone Monotherapy Versus Prednisolone Plus Methotrexate in Erythema Nodosum Leprosum (Type 2 Lepra Reaction)

研究概览

简要总结

Erythema nodosum leprosum (ENL) is characterized by painful nodules and systemic compromising. It is usually recurrent and/or chronic and has both physical and economic impact on the patient, being a very important cause of morbidity and mortality. In addition, ENL is a major health problem in developing countries like Bangladesh where leprosy is endemic. Therefore, adequate control of this condition is important to reduce morbidity and mortality.

The treatment of ENL is usually started with steroids which have many adverse effects when given for prolonged periods and in high doses. However, recently in some case reports MTX appears to have a beneficial effect in cases of ENL. Also, MTX may provide a cheaper and convenient option in management of ENL.

However, there is paucity of well-designed randomized controlled trial on the effectiveness of MTX in the treatment of ENL. In this context such studies are needed. The investigator therefore designed this randomize trial to evaluate the efficacy and safety of combined MTX and Prednisolone over Prednisolone monotherapy in local setting. The investigator combined reducing doses of Prednisolone with a low dose MTX to minimize dose related complications, while maximizing benefit in controlling ENL. If the study results would show the superiority of combined regimen as found elsewhere in the World, it would be helpful to reduce the morbidity of ENL Patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient with ENL had crops of tender subcutaneous skin lesions with systemic features including fever (temperature >38°C), neuritis, joint pain, bone tenderness, orchitis, iritis, oedema, malaise, anorexia and lymphadenopathy.
  • Patients of both sexes with age ranging 18 years to 65 years.

排除标准

  • Erythema nodosum associated with other disorder.
  • Pregnant and lactating women.
  • Diagnosed case of chronic hepatic, renal, hematological or other connective tissue disorders, Osteoporosis.
  • Severely ill, immune-suppressed patients like HIV/AIDS and patients of internal malignancy.
  • Patients or guardians not willing to participate in the study by signing informed consent form.

研究组 & 干预措施

oral Prednisolone alone

Experimental

10 patient

干预措施: Efficacy and Safety of Prednisolone Monotherapy Versus Prednisolone Plus Methotrexate in Erythema Nodosum Leprosum (Type 2 Lepra Reaction) (Drug)

oral Methotrexate plus Prednisol

Experimental

9 patient

干预措施: Efficacy and Safety of Prednisolone Monotherapy Versus Prednisolone Plus Methotrexate in Erythema Nodosum Leprosum (Type 2 Lepra Reaction) (Drug)

结局指标

主要结局

Efficacy and Safety of Prednisolone Monotherapy Versus Prednisolone Plus Methotrexate in Erythema Nodosum Leprosum (Type 2 Lepra Reaction)

时间窗: 01.06.2018 to 31.12.2019 total 18 months

Primary outcome: Improvement in Reaction severity assessment score by observing signs and symptoms like tender skin ENL nodules.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mohammad Rafiqul Mowla

MBBS, MD, PHD

Chittagong Medical College

研究点 (1)

Loading locations...

相似试验

Prednisolone Monotherapy Versus Prednisolone Plus... | 临床试验