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Clinical Trials/CTRI/2023/06/053385
CTRI/2023/06/053385
Not yet recruiting
Phase 2

An Anatomico-clinical study on comparative effect of Gulpha Marma Chikitsa & Yavani Churna in Primary Dysmenorrhoea (Krichhartava)

Faculty of Ayurveda IMS Banaras Hindu University0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: N944- Primary dysmenorrhea

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: N944- Primary dysmenorrhea
Sponsor
Faculty of Ayurveda IMS Banaras Hindu University
Status
Not yet 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
Faculty of Ayurveda IMS Banaras Hindu University

Eligibility Criteria

Inclusion Criteria

  • •1Patients willing to participate in study.
  • •2Age group between 14 to 45 years.
  • •3Unmarried and married both patients attending the OPD with chief complain of Primary Dysmenorrhoea with scanty or average amount of menses along with associated symptoms without any organic pathology.
  • •4patients suffering more than two cycles.

Exclusion Criteria

  • •1Patients below 14 years and above 45 years.
  • •2Any abnormalities detected in investigation.
  • •3Coagulation disorders.
  • •4Patients suffering from chronic systemic disease like uncontrollable diabetes, uncontrollable hypertension, venereal disease, thyroid dysfunction or any disorders influencing general physical health and ultimately influencing menses.
  • •5Patients using IUCD and OCPs or injectables contaceptive and others.
  • •6Patients with any history of allergy or allergy from trial drugs.
  • •7Patients having Central nervous system disorders like epilepsy, meningitis, migraine or any other psychological disorders.
  • •8Patients having Respiratory disorders like bronchial asthma, T.B., pleural effusion, bronchitis etc.
  • •9Patients having any carcinoma.

Outcomes

Primary Outcomes

Not specified

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