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临床试验/NCT01056042
NCT01056042已完成4 期

Postoperative Intramuscular Depot Medroxyprogesterone Acetate Versus Continuous Oral Contraceptive for Pelvic Pain Associated With Endometriosis : Randomized Comparative Trial.

Prince of Songkla University1 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2007年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
112
试验地点
1
主要终点
Patients' satisfaction with the treatment

研究概览

简要总结

Patients with endometriosis-associated pain have conservative surgery performed to remove all visible lesions. Then, patients are randomized into two groups. In the first group patients have depot medroxyprogesterone acetate injections every 3 months for a total of 6 months.In the second group patients have oral contraceptive combined pills everyday for 6 months. Patients are followed up on recurrence of pain for 1 year after medication.

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 (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Premenopausal women from 18 to 45 years of age with endometriosis-associated pain for at least 6 months who had conservative surgery performed.

排除标准

  • Medical therapies for endometriosis other than NSAID within previous 6 months
  • Contraindication to the drugs
  • Wish to conceive
  • Request for extirpative surgery
  • Other pelvic pathology ( adenomyosis, chronic PID, submucous myoma uteri )

研究组 & 干预措施

A

Experimental

Intramuscular depot medroxyprogesterone acetate

干预措施: intramuscular depot medroxyprogesterone acetate (Drug)

B

Active Comparator

ethinyl estradiol 30 micrograms combined with gestodene 75 micrograms

干预措施: ethinyl estradiol 30 micrograms, gestodene 75 micrograms (Drug)

结局指标

主要结局

Patients' satisfaction with the treatment

时间窗: 1 year and 6 months

次要结局

  • pain reduction and adverse side effects(1 year and 6 months)

研究者

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

Sopon Cheewadhanaraks

Associate Professor

Prince of Songkla University

研究点 (1)

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