A Clinical trial to study the effect of Patha (Cissampelos pariera) in patients with painful menstruation.
Not yet recruiting
- Conditions
- Primary dysmenorrhea. Ayurveda Condition: kashtartava,
- Registration Number
- CTRI/2021/09/036512
- Lead Sponsor
- Himani
- Brief Summary
this study is randomized open interventional study, to measure the efficacy of decoction of *patha* given at a dose of 50 ml twice a daily for three menstrual cycles that will be conducted in a single centre in india. The primary outcome measures will be the pacification or complete resolution of primary dysmenorrhea by decoction of *patha.* The secondary outcome will be no efficacy of decoction of patha in managing the pain of primary dysmenorrhea.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Female
- Target Recruitment
- 30
Inclusion Criteria
Patients or parents of the young patients who agree to give written consent patients having chief complaint of painful menses patient suffering from primary dysmenorrhoea for more than 3 cycles.
Exclusion Criteria
- Patients or parents of the young patients who do not agree to give written consent.
- Patient with chronic systemic illness and uterine pathology like fibroid, adenomyosis, endometriosis.
- Patient with intrauterine contraceptive devices.
- Patient suffering from hypothyroidism or Hyperthyroidism.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Menstruation is not painful anymore or is reduced to a substantial amount. 3 Months
- Secondary Outcome Measures
Name Time Method Menstruation is still painful to the same extent as before Intervention. 3 Months
Trial Locations
- Locations (1)
Government Ayurvedic Hospital, Patiala
🇮🇳Patiala, PUNJAB, India
Government Ayurvedic Hospital, Patiala🇮🇳Patiala, PUNJAB, IndiaHimaniPrincipal investigator7413055970himania007@gmail.com