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Clinical Trials/CTRI/2023/05/053271
CTRI/2023/05/053271
Recruiting
Phase 2

A COMPARATIVE CLINICAL STUDY TO EVALUATE THE EFFICACY OFVAMANA KARMA AND VAMANA KARMA FOLLOWED BY NASYA KARMA IN THE MANAGEMENT OF ARTAVAKSHAYA W.S.R. TO PCOS

Parul Ayurved Hospital0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: E282- Polycystic ovarian syndrome

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: E282- Polycystic ovarian syndrome
Sponsor
Parul Ayurved Hospital
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Parul Ayurved Hospital

Eligibility Criteria

Inclusion Criteria

  • •â®?Both married / unmarried females in age group of 18\-40 years
  • •â®?Patients having symptoms of PCOS (any two given by ASRM \& ESHRE)
  • •â®?Oligomenorrhea and /or Anovulation
  • •â®?Polycystic Ovaries.
  • •â®?Patients indicated for Vamana karma
  • •â®?Patients indicated for Nasya karma

Exclusion Criteria

  • •1\. Patients contraindicated for Vamana karma
  • •2\. Patients contraindicated for Nasya karma
  • •3\. Cervical tumour, polyp, carcinoma of cervix.
  • •4\. Uterine fibroid,
  • •5\. Congenital anomalies of female genital tract
  • •6\. Chronic illness

Outcomes

Primary Outcomes

Not specified

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