A pilot study on the efficacy of oral satavar and vaginal pessary of camphor and Rogan e gul in the management of Vaginal dryness
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 10
- 试验地点
- 1
- 主要终点
- 1.change in vaginal dryness severity from baseline to end of treatment measured using Vas score or vaginal dryness self assessment scale
研究概览
简要总结
A pilot study on the efficacy of oral satavar and vaginal pessary of Rogan e gul and camphor in the management of Vaginal dryness
Aim : To evaluate the effectiveness of oral satavar ( Asparagus racemosus ) in combination with vaginal pessary of camphor and Rogan e gul in the management of Vaginal dryness among Post menopausal woman.
Inclusion criteria:
1.woman aged 40-60 years.
- Presence of at least one symptoms such as itching,burning,discomfort or pain during intercourse for at least past 3 months.
3.menopausal status
Postmenopausal woman ( greater than 12 months since last menstrual period)
- No use of systemic estrogen therapy, hormonal contraceptive or vaginal lubricant for at least 2 weeks prior to study initiation
Exclusion criteria:
- Presence of vaginal or urinary tract infection
2.pelvic organ prolapse, severe atrophic vaginitis
-
Use of systemic estrogen
-
Use of vaginal lubricant
Primary outcome:
Change in vaginal dryness severity from baseline to end of treatment measured using Vas score or vaginal dryness self assessment scale
Secondary outcome
Associated symptoms improvement ( reduction in itching, burning)
Interventions:
Test group
- Oral satavar (Asparagus racemosus)
Patient will be given 6gm of above mentioned drug powder per day for 90 days
- Vaginal pessary of camphor and Rogan e gul
Patient will be given vaginal pessary of above mentioned drug per day for 10 days for 3 consecutive months.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 40.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- Female
入选标准
- •Presence of at least one symptoms such as itching burning discomfort or pain during intercourse for at least past 3 months
- •Menopausal status: a.postmenopausal woman (greater than 12 months since last menstrual period) 3.no use systemic or local estrogen therapy hormonal contraceptive or vaginal lubricant for at least 2 weeks prior to study initiation.
排除标准
- •Presence of vaginal or urinary tract infection 2.pelvic organ prolapse, severe vaginal atrophy with ulceration 3.use of systemic estrogen 4.use of vaginal lubricant.
结局指标
主要结局
1.change in vaginal dryness severity from baseline to end of treatment measured using Vas score or vaginal dryness self assessment scale
时间窗: 90 days
次要结局
- Associated symptoms improvement ( reduction in itching, burning)(90 days)
研究者
Dr Amreen Begum
Government nizamia tibbi college and general hospital