A RANDOMISED CONTROLLED CLINICAL TRIAL TO EVALUATE THE EFFICACY OF KUMARI SIDDHA TAILA MATRABASTI AND SHATPUSHPA SIDDHA TAILA MATRABASTI IN ANOVULATORY CYCLE IN ANOVULATORY CYCLE IN PCOS
Overview
- Phase
- Phase 2/3
- Status
- Not yet recruiting
- Sponsor
- Tilak ayurvedic mahavidyalaya rasta peth Pune
- Enrollment
- 50
- Locations
- 1
- Primary Endpoint
- The study will analyze the clinical signs and symptoms to determine the effectiveness of each treatment.
Overview
Brief Summary
The study will be intervened by the treatment of Kumari siddha tail matra basti and Shatpushpa siddha taila matra basti to group A and group B respectively. The efficacy of the
therapy will be assessed on the basis of subjective and objective criteria for statistical
analysis. Scoring will be designed according to the severity of symptoms. The
subjective and objective gradation of symptoms will be done as follows and the
intensity of each symptom will be calculated before treatment, after treatment and
after follow up. The effect of treatment result will be assessed in regards to clinical
signs and symptoms on the basis of grading and scoring system. The signs and
symptoms will be assessed by adopting the suitable scoring method.
Study Design
- Study Type
- Interventional
- Allocation
- Coin toss, Lottery, toss of dice, shuffling cards etc
- Masking
- None
Eligibility Criteria
- Ages
- 18.00 Year(s) to 35.00 Year(s) (—)
- Sex
- Female
Inclusion Criteria
- •Age group 18-35 years.
- •Diagnosis Ultrasound Polycystic ovarian morphology.
- •Diagnosed cases of PCOS with any of the following symptoms Ovulatory dysfunction refers to Oligomenorrhea or amenorrhea.
- •Anovulatory Cycles Irregular Menses/ Scanty Menses.
- •Hirsutism Obesity Acanthosis Nigricans.
Exclusion Criteria
- •Patients having history of Systemic diseases like Diebetes mellitus, Hypertension, etc.
- •Irregular menses due to anatomical defect in reproductive system such as Hypoplastic Uterus, Aplastic Uterus, Streak Ovaries, Hypogonadism.
- •Menorrhagia in PCOS.
Outcomes
Primary Outcomes
The study will analyze the clinical signs and symptoms to determine the effectiveness of each treatment.
Time Frame: 12 weeks
Secondary Outcomes
- No any(No ANY)
Investigators
DrSampada Anil Shinde
Tilak ayurvedic mahavidyalaya rasta peth pune