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临床试验/NCT00369018
NCT00369018已完成1 期

Methyl Aminolevulinate (MAL) and Hexaminolevulinate (HAL) Photodynamic Therapy (PDT)of Cervical Intraepithelial Lesions (SIL) - a Double-blind Dose-finding Study

Photocure2 个研究点 分布在 2 个国家目标入组 96 人开始时间: 2006年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
96
试验地点
2
主要终点
Lesion eradication

研究概览

简要总结

The study will determine the best drug (MAL or HAL) dosage for photodynamic therapy of cervical precancerous lesions (dysplasia) in women that are referred for conisation (surgery).

详细描述

Surgery (conisation) of precancerous cervical lesions (dysplasia) increase the risk of preterm deliveries in young women. Photodynamic therapy (PDT) is a selective, tissue preserving method that may become a good treatment option for these patients.

This study will explore topical application of methyl aminolevulinate (MAL) and hexaminolevulinate (HAL) of the cervix for photodynamic therapy using red light (630 nm). Different doses of MAL and HAL will be used with different application time, followed by illumination.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Positive histology of CIN 1-3

排除标准

  • Patients with endocervical lesions
  • Patients with AGUS
  • Patients with invasive disease
  • Patients with porphyria
  • Patients sensitive to MAL and HAL

研究组 & 干预措施

MAL 3

Active Comparator

干预措施: methyl aminolevulinate (MAL) and hexaminolevulinate (HAL) (Drug)

MAL 12

Active Comparator

干预措施: methyl aminolevulinate (MAL) and hexaminolevulinate (HAL) (Drug)

HAL 10, 3

Active Comparator

干预措施: methyl aminolevulinate (MAL) and hexaminolevulinate (HAL) (Drug)

HAL 10, 12

Active Comparator

干预措施: methyl aminolevulinate (MAL) and hexaminolevulinate (HAL) (Drug)

HAL 40, 3

Active Comparator

干预措施: methyl aminolevulinate (MAL) and hexaminolevulinate (HAL) (Drug)

HAL 40, 12

Active Comparator

干预措施: methyl aminolevulinate (MAL) and hexaminolevulinate (HAL) (Drug)

结局指标

主要结局

Lesion eradication

时间窗: 6 months

次要结局

  • Eradication of lesion and HPV(6 and 12 months)
  • Safety assessment(6 months)

研究者

发起方
Photocure
申办方类型
Industry

研究点 (2)

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