Non-surgical Interventions for Infertility in Endometriosis: A Parallel-Design Randomized Clinical Trial
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 18
- 试验地点
- 1
- 主要终点
- Pain reduction estimated by mean change on a Visual Analog Scale
研究概览
简要总结
A parallel design randomized clinical trial was carried out on 18 women with clinically diagnosed endometriosis who wish pregnancy in the Department of Reproductive Endocrinology and Infertility, Bangabandhu Sheikh Mujib Medical University, (BSMMU), Shahbag, Dhaka. Those who voluntarily provide consent to participate in this study will be randomly allocated to one of the two treatment arms. Allocation concealment will be done by sequentially numbered sealed envelopes. The arms and interventions are cabergoline (0.5 mg twice weekly for 6 months, plus timed intercourse) and dydrogesteron (20 mg daily from day 5 to day 25 of menstrual cycle for 6 months, plus timed intercourse).The women will be assessed by telephone interview at monthly intervals, TVS and serum Ca 125 at 3 months and 6 months.
详细描述
Infertile women with endometriosis will be recruited from those attending Dept of Reproductive Endocrinology and Infertility after clinical diagnosis on the basis of sonographic findings of chocolate cyst with or without dysmenorrhea. After evaluating for eligibility criteria and taking informed consent she will be randomized to either cabergoline group or to dydrogesterone group. Women assigned to cabergoline group will receive 0.5 mg cabergoline twice weekly (fridays and tuesdays), after meal at night for 6 months. The dydrogesterone group will receive 10 mg of dydrogesterone twice daily from day 5 to day 25 of menstrual cycle for six months. She will be followed up every month to check for compliance or any side effects. The couple will have intercourse timed with LH kit or intercourse on alternate days from day 10 to day 15 of the cycle if the LH kit is not available. She will visit 3 months and 6 months after the beginning of treatment. At each follow up visit, she will be assessed for pregnancy, visual analog scale for pain and transvaginal sonogram to measure the chocolate cyst. Estimation of serum CA125 and any side effects will be noted.
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
- None
入排标准
- 年龄范围
- 18 Years 至 35 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Women of reproductive age 18-35 yrs
- •Women who are infertile or wish pregnancy
- •Sonographic diagnosis of chocolate cyst with or without dysmenorrhea
- •Women staying with her husband
排除标准
- •Recurrent endometrioma after previous surgery
- •BMI at or more than 30 kg/m2
- •Significant abnormalities in renal and liver function.
- •Known male factor
- •Use of investigational drugs or hormones, concomitant or in last 30 days.
研究组 & 干预措施
Cabergoline
Tab Cabergoline 0.5 mg twice weekly for 24 weeks, plus timed intercourse
干预措施: Cabergoline plus timed intercourse (Drug)
Dydrogesterone
tab Dydrogesterone( 10 mg) twice daily from day 5 to day 25 of menstrual cycle for 24 weeks, plus timed intercourse
干预措施: Dydrogesterone plus timed intercourse (Drug)
结局指标
主要结局
Pain reduction estimated by mean change on a Visual Analog Scale
时间窗: 24 weeks
Mean change in Visual Analogue Score (1-10), higher score means worse outcome
Percentage change in size
时间窗: 24 weeks
Percentage change in size (maximum diameter) of chocolate cyst assessed by transvaginal ultrasound at week 24
Pregnancy rate
时间窗: 24 weeks
Proportion in each group of participants of those who conceive , biochemical (serum beta hCG \> 40 IU/mL) or clinical (sonographic appearance of gestational sac)
次要结局
- Change in CA 125(24 weeks)
- Adverse effect(24 weeks)
研究者
Shakeela Ishrat
Associate Professor, Department of Reproductive Endocrinology & Infertility
Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh