Status:

NOT_YET_RECRUITING

Combined Effect of Therapeutic Ultrasound and Trans Cutaneous Electrical Nerve Stimulation on Endometriosis

Lead Sponsor:

Cairo University

Conditions:

Endometriosis

Eligibility:

FEMALE

25-35 years

Phase:

NA

Brief Summary

This study will be conducted to investigate the combined effect of therapeutic ultrasound and transcutaneous electrical nerve stimulation (TENS) on relieving adhesions and pain related to endometriosi...

Detailed Description

Endometriosis affects 10-15% of reproductive-age women, causing pelvic pain and infertility. While laparoscopy is the primary treatment, it has risks. Medications are also used but often have side eff...

Eligibility Criteria

Inclusion

  • Forty-five women clinically diagnosed by the gynecologist with endometriosis will be included in the study.
  • Abdominal wall endometriosis will be diagnosed via Color Doppler ultrasonography.
  • Their ages will range from 25 to 35 years old.
  • Their body mass index (BMI) will be ranged from 25 to 35 Kg/m2.
  • All patients have reported mild to moderate endometriosis symptoms such as (chronic pelvic pain (CPP), dysmenorrhea, dyspareunia, pain with bowel movements and urination and excessive bleeding) as recorded by Endometriosis Health profile questionnaire (EHP30).
  • All patients use continuous hormonal treatment for at least 3 months.

Exclusion

  • Severe endometriosis which is diagnosed by the gynecologist.
  • Pregnancy, peacemaker, epilepsy, cardiac arrhythmia, cancer, acute inflammatory pelvic disease.
  • Use of injectable hormonal therapy within the previous 6 weeks.
  • Patients with contraindication of ultrasound (Patients with reduced sensation to pain and/or heat, local malignancy, local acute infection and over areas of thrombosis or other vascular abnormalities).
  • Cognitive deficiency and difficulty to understand instructions or use the instruments.

Key Trial Info

Start Date :

August 10 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

October 10 2024

Estimated Enrollment :

45 Patients enrolled

Trial Details

Trial ID

NCT06537765

Start Date

August 10 2024

End Date

October 10 2024

Last Update

August 6 2024

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