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Clinical study of Unani Formulation in patients of pain during menstruatio

Phase 2
Conditions
Health Condition 1: N944- Primary dysmenorrhea
Registration Number
CTRI/2024/07/070202
Lead Sponsor
Faiza Furqan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients of age group 12 35 years

Patients with regular painful menstruation maybe associated with one or more symptoms like Nausea vomiting diarrhea fatigue

Patients with regular and irregular menstrual cycle

Patients strictly with primary dysmenorrhea

Patients willing to take part in the study

Exclusion Criteria

Patients of age less than 12 and more than 35 years

hormonal and metabolic disorders any organic pelvic pathology

sensitivity to NSAID

Any systemic diseases like hypertension diabetes mellitus and sexually transmitted disease Patients with irregular cycle and flow

Patients with secondary dysmenorrhea

Lactating women

If the subject not willing to continue

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
decrease in VAS and VMSS scores for pain intensityTimepoint: 3 consecutive menstrual cycle
Secondary Outcome Measures
NameTimeMethod
improvement in the quality of life determined by SF 36 health survey questionnaire reduction in the duration of pain associated systemic symptoms and PBLAC score for menstrual blood lossTimepoint: 3 consecutive menstrual cycle
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