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Clinical Trials/CTRI/2021/04/032668
CTRI/2021/04/032668
Recruiting
Phase 2

An open Double arm Randomized Comparative Clinical trial toEvaluate and Compare the Efficacy of Siddha herbal formulationsKalingadhy thailam and Inji Churanam in reducing pain among theReproductive age group with Dhoorasoolai (Primary dysmenorrheaNSMC Code: ZAA1.8) at SCRI OPD Chennai- A pilot study. - EKIPD

Central Council for Research in Siddha0 sites0 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium
Sponsor
Central Council for Research in Siddha
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Central Council for Research in Siddha

Eligibility Criteria

Inclusion Criteria

  • 1 Trial participants who are at the age group of 18\-35 years
  • 2 Menstrual pain for more than 3 consecutive regular menstrual cycle without pelvic organ pathology
  • 3 Complaints of primary dysmenorrhea from menarche or shortly after (6ââ?¬â??24 months) menarche.
  • 4 Regular menstrual cycle of 24 to 32 days
  • 5 Severe dysmenorrhea with 8\-12 score using WaLLID tool

Exclusion Criteria

  • 1 Study participants who have pelvic inflammatory diseases
  • 2 Irregular menstrual cycle
  • 3 Secondary dysmenorrhea associated with ovarian cyst, endometriosis and fibroid (excluded clinically and radio logically)
  • 4 Pain abdomen associated with excessive BPV
  • 5 Having oral contraceptive pills and IUCD (Intrauterine contraceptive pills)
  • 6 Who are under the treatment of hormonal therapy
  • 7 who are pregnant/planning to pregnant, Lactating mother

Outcomes

Primary Outcomes

Not specified

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