A study to Check For Effectiveness Of Nasya treatment in the management of Anovulation Condition In PCOD

A Randomised Clinical Trial To Evaluate The Efficacy Of Shigru Beejadi Ghruta And M D Forte Taila Nasya In The Management Of Anovulation In Polycystic Ovarian Disease PCOD - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/06/088499

Enrollment

Registered

2025-06-10

Start date

Unknown

Completion date

Unknown

Last updated

2025-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: E282- Polycystic ovarian syndrome

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Married women 2.Irregular menses 3.Hyperandrogenism 4.Polycystic ovaries

Exclusion criteria

Exclusion criteria: 1. Patients with primary amenorrhea. 2. Endocrinological disorders like Diabetes Mellitus, Thyroid abnormalities, Congenital Adrenal Hyperplasia and Hyperprolactinemia. 3. Chronic systemic diseases which can interfere with the treatment. 4. Any malignancy of Breast or cervical or ovarian origin. 5.Patients on oral contraceptive pills, IUCD, injectable contraceptives. 6. USG showing Congenital or Acquired Anatomical defects, Pelvic pathology. 7.Pregnant and lactating mothers. 8.Those contraindicated for Pratimarsha Nasya.

Design outcomes

Primary

Measure	Time frame
Assesed based on subjective and objective parameters Subjective Parameters Quantity of menses 2.Duration of bleeding 3.Interval between the menstrual cycles 4.Pain during menses Objective parameters 1.Hirsutism score 2.GAGS score scale 3.ANSC scoring chart 4.BMI and Weight Reduction, and WHR. 5.Vas Score 6.WaLIDD score 7.USG of pelvis for ovarian follicular study, endometrial thickness and to assess ovulation BT once and at the end of the study (3rd M). Timepoint: Follicular study will be done for 3 months to check ovulation and final assessment will be done on 3rd month of study	—

Measure

Time frame

Assesed based on subjective and objective parameters Subjective Parameters Quantity of menses 2.Duration of bleeding 3.Interval between the menstrual cycles 4.Pain during menses Objective parameters 1.Hirsutism score 2.GAGS score scale 3.ANSC scoring chart 4.BMI and Weight Reduction, and WHR. 5.Vas Score 6.WaLIDD score 7.USG of pelvis for ovarian follicular study, endometrial thickness and to assess ovulation BT once and at the end of the study (3rd M). Timepoint: Follicular study will be done for 3 months to check ovulation and final assessment will be done on 3rd month of study

—

Secondary

Measure	Time frame
NilTimepoint: Nil	—

Countries

India

Contacts

Public ContactPawar Sankirna Appu

Alvas Ayurveda Medical College,Moodbidrie

drasokan24@gmail.com9148185776

Outcome results