Effect of Leech Therapy and Dry cupping on Polycystic Ovary Syndrome

Phase 3

Recruiting

Conditions: Polycystic Ovary Syndrome.
Polycystic ovarian syndrome
E28.2

Registration Number: IRCT20200623047903N1

Lead Sponsor: Gonabad University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Female

Target Recruitment: 40

Inclusion Criteria

The Polycystic Ovaries based on the individual's satatement
Having Written and oral consent to participate in the study
Age range of 18 to 40
Having reading and writing Literacy
Body mass index Between 18.5 to 24.9
Lack of drug use
No having chronic physical disease
They did not Receive any Treatment for Polycystic Ovaries for 6 Months ago
Failing to use hormonal drugs during the study
Do not Take Hormonal Medications During the Study
Patients with Stable Medical Condition
Not Pregnant
No Breastfeeding
People with Oligomenorrhea

Exclusion Criteria

Individual Intolerance to Leeches or Dry Cupping or LD

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The Duration of the Menstrual cycle. Timepoint: Before the Intervention, 1 Month, 2 and 3 Months after the Intervention. Method of measurement: A Researcher-made Questionnaire and Calendar.;Menstrual Bleeding Volume. Timepoint: Before the Intervention, 1 Month, 2 and 3 Months after the Intervention. Method of measurement: Blood Visual Assessment Questionnaire.;The Severity of Menstrual Cramps. Timepoint: Before the Intervention, 1 Month, 2 and 3 Months after the Intervention. Method of measurement: Visual Analogue Scale.

Secondary Outcome Measures

Name	Time	Method
Satisfaction with Treatment. Timepoint: After the Intervention. Method of measurement: Questionnaire.;Complications. Timepoint: After the Intervention. Method of measurement: Check list.