The effect of using Biophilia Lotus nls device on the treatment of endometriosis in patients referred to Fatemieh hospital clinic in 2024.
Conditions
Interventions
Intervention 1: Intervention group: First, the conditions of the study were fully explained to all patients and written informed consent was obtained from them. All patients are diagnosed with endome
Sponsors
Hamedan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: Women in the age range of 20-50 years with confirmed endometriosis
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Abdominal pains. Timepoint: Patients are diagnosed with endometriosis with Biophilia Lotus NLS bioresonance device and then are treated with this device. Patients in the intervention group are treated for 10 sessions with an interval of 48 hours. The control group was also among the participants who visited the clinic and had a definite diagnosis of endometriosis by ultrasound and were subjected to routine treatment (drug treatment). The number of abdominal pains during the cycle in the intervention and control groups is checked before starting treatment with the device and routine treatment. The next evaluation will be done after the end of 10 sessions, 30 days after the start of the treatment in two groups. Then a comparison will be made between the two groups. Method of measurement: The frequency of abdominal pain and its intensity with a scale with numbers between 0-10 with visual analog scale (VAS).;Bleeding intensity. Timepoint: Patients are diagnosed with endometriosis with Biophilia Lotus NLS bioresonance device and then are treated with this device. Patients in the intervention group are treated for 10 sessions with an interval of 48 hours. The control group was also among the participants who visited the clinic and had a definite diagnosis of endometriosis by ultrasound and were subjected to routine treatment (drug treatment). Heavy bleeding in the intervention and control groups are all checked before starting treatment with the device and routine treatment. The next evaluation will be done after the end of 10 sessions, 30 days after the start of the treatment in two groups. Then a comparison will be made between the two groups. Method of measurement: The researcher-made checklist includes questions about the amount of bleeding with numbers between 0-10. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactLeila Hekmat
Hamedan University of Medical Sciences
Outcome results
None listed