A trial drug for Polycystic Ovarian disease
- Conditions
- Irregular Menstrual cycles
- Registration Number
- CTRI/2014/06/004709
- Lead Sponsor
- National Institute of Siddha
- Brief Summary
This is a single arm open clinical trial to find out the therapeutic effect of Karpagandhi ennai (Internal). The trial drug is a combination of herbomineral drugs from the Siddha Text book Anubhava Siddha Vaidhya Muraigal (Author Balaraamayya )for the namagement of Sinaipaineerkatti (PCOS) in women. The constituents of the trial drug are Gandhagam (Sulphur), Poondu (Allium sativum), Gingelly oil (Seasamum indicum). The internal drug will be issued in oil form at a dosage of 5 drops once a day with half-baked egg yolk for 10 days thereafter the drug will be stopped for next 10 days and restarted for 10 days. Likewise drug will be given for 30 days for a patient. The clinical assessment and laboratory investigations will be recorded before and after the treatment period. All the trial related data will be recorded, analysed statistically and the research reports will be published.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 10
- •Irregular menstrual cycle: Eight or fewer menstrual cycles in the past year or intermenstrual periods of 45 days or longer.
- •Patients having polycystic ovary on ultrasound should either have 12 or more follicles measuring 2-9 mm in diameter, or have an increased ovarian volume of 10 CC or greater •Patient willing for Ultrasound abdomen and blood investigations.
- •Patient willing to sign the informed consent.
- •Presence of any pelvic pathology such as chronic pelvic infection, Pelvic endometriosis, Adenomyosis, Uterine fibroid, Endometrial Polyp.
- •Presence of secondary endocrine disorder such as hyperprolactinaemia, thyroid dysfunction.
- •Patient using oral contraceptives or use of fertility drugs within 6 months •Presence of any associated severe systemic illness.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method •Normal appearing of ovary confirmed by TV USG or Confirming of normal follicles being formed and ruptured through folliculogram. 6-9 months •Establishing regularization of menstrual cycle. 6-9 months
- Secondary Outcome Measures
Name Time Method •Enhancing weight reduction with a BMI 30. •Reducing elevated hormone levels like testosterone and DHEAS.
Trial Locations
- Locations (1)
National Institute of Siddha
🇮🇳Chennai, TAMIL NADU, India
National Institute of Siddha🇮🇳Chennai, TAMIL NADU, IndiaSKeerthanaPrincipal investigator9962927684sk.keerthana@gmail.com