Health Condition 1: N889- Noninflammatory disorder of cervixuteri, unspecified
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patient Willing To Give Voluntary Informed Consent Age Group Between 16-35 Years Both Married And Unmarried Women Pain In The Lower Abdomen Which Begin One Or Two Days Before Menstruation Or With The Onset Of Menstruation And Lasting For Few Hours Or One To Two Days Painful Menstruation Also Associated With Symptoms Like Nausea Vomiting Constipation Etc History Of Painful Menstruation For Atleast 3 Consecutive Cycles Patient Diagnosed With Dysmenorrhoea Patient With Regular Menstrual Cycle 21 To 35 Days
Exclusion criteria
Exclusion criteria: Patient Who Is Not Willing To Give Voluntary Informed Consent Patients Taking Any Hormonal Therapy Patients Of Any Pelvic Pathology PCOD PID Cervical stenosis Fibroid Endometriosis Adenomyosis Etc Patients With Congenital Anomalies Of Reproductive System Other Medical Disorders Which Make Patients At High Risk Like Epilepsy Anaemia Hb Less Than 8mg/dl Heart Disease DM Surgical And Malignant Conditions Heavy Bleeding During Menses Patients Are Excluded More Than 4 Pads Fully Soaked Per Day
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change In The Grade Of VAS Visual Analogue Score Scale Of PainTimepoint: Follow Up Will Be Done on Day 4 Of Three Consecutive Cycles And 120th day | — |
Secondary
| Measure | Time frame |
|---|---|
| CHANGES IN OTHER ASSOCIATED CLINICAL SYMPTOMS LIKE NAUSEA VOMITING ETCTimepoint: Follow Up Will Be Done On Day 4 Of Three Consecutive Cycles And 120th day | — |
Countries
India
Contacts
Institute For Ayurved Studies And Research