A clinical trial on dysmenorrhea
Phase 2
Completed
- Conditions
- Health Condition 1: null- pain present in the lower abdomen during mensturation
- Registration Number
- CTRI/2018/02/012037
- Lead Sponsor
- ational institute of siddha
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 10
Inclusion Criteria
Age between 11 to 25 years.
Nulliparous women.
Patient willing to Ultrasound abdomen and blood investigations.
Spasmodic dysmenorrhoeal pain ranging from 4-10 according to Numerical Rating Pain Scale.
Patient willing to sign the informed consent
Exclusion Criteria
Presence of any pelvic pathology such as Chronic pelvic infection, Pelvic endometriosis, Adenomyosis, Uterine fibroid, Endometrial Polyp,
IUCD in utero.
Presence of any associated severe systemic illness.
Abdominal pain presenting other than the period of menstruation.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Significant outcome - Reduction of lower abdominal pain from 4-10 to 0 in the pain scale <br/ ><br>Good outcome - Reduction of pain from 7-10 to1 â?? 3 <br/ ><br>Moderate outcome - Reduction of pain from 4-6 to1 â?? 3 and from 7-10 to 4-6. <br/ ><br>Timepoint: 3-5 days of menstruation and premenstrual period <br/ ><br>
- Secondary Outcome Measures
Name Time Method Reduction in the menstrual pain in successive 3 cyclesTimepoint: 3 months