CTRI/2024/03/063422
Not yet recruiting
Phase 2
A Comparative Clinical Study on the Therapeutic Effect of Guduchyadi Taila Uttar Basti and Rasnadi Ksheerpaka Orally in Vataja Yonivyapad - No
Department of Prasuti Tantra0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Health Condition 1: N946- Dysmenorrhea, unspecified
- Sponsor
- Department of Prasuti Tantra
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Married women of 20\-40 years of age.
- •2\. Patient having complaint of pain during menses along with one or more than one symptomatology from the following at least two previous consecutive cycle\-
- •(a)Pain in abdomen during menses.
- •(b)Decrease duration of menstrual blood \[duration of blood loss is 2 days or less than 2 day].
- •(c)Decrease amount of menstrual blood \[quantity of menstrual is less than 20ml].
- •(d)With thin, dry, frothy characteristic of menstrual blood.
- •(e)Sensory symptoms numbness, roughness or stiffness in genital region.
- •(f)Associated symptoms nausea, vomiting, bodyache, headache.
Exclusion Criteria
- •1\.Women below 20 years and above 45 years of age.
- •2\.Unmarried or Pregnant women
- •3\.Women with systemic diseases like TB, DM, Jaundice, Bronchial Asthma, Cardiovascular diseases, Renal diseases or Acute gastrointestinal conditions like Appendicitis, Cholecystitis, Hepatitis, pancreatitis, gastric ulcer.
- •4\.Women having complaint of Menorrhagia.
- •5\.Patients having STD, Carcinoma of Cervix, Large cervical polyp, Acute active genital infections, bartholin abscess, Large bartholin cyst, large vaginal cyst, large, polypoidal fibroid, Uterine prolapse (2or 3degree), extensive ectropion.
- •6\.Skin disease in perineal region like eczema, herpes.
- •7\.Patient is on chemotherapy / radio therapy for any malignant condition of any organ.
- •8\.Women having any psychological disorders.
- •9\.Women having lactose intolerance.
Outcomes
Primary Outcomes
Not specified
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