Immediate effect of an electrostimulation session for Menstrual Cramp pai

Not Applicable

Recruiting

• Conditions: Primary dysmenorrhea; C23.550.568

• Registration Number: RBR-10vpc86k
• Lead Sponsor: niversidade Federal de São Carlos

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-10-13
• Last Update Posted: 13 November 2023
• Study Completion: 2024-08-31

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Women without children; aged between 18 and 45 years; with regular menstrual cycle; with primary dysmenorrhea assessed with 3 points or more for dysmenorrhea pain intensity by Numerical Pain Scale (END); and who had never had previous contact with Transcutaneous Electrical Nerve Stimulation (TENS).

Exclusion Criteria

Pregnant women; postpartum women up to 6 months after delivery; women using an intrauterine device; presence of skin lesions at the electrode application site; with self-reported neurological and/or heart diseases; diagnosis of gynecological disorders (such as endometriosis, uterine fibroids, etc.) that may be related to secondary dysmenorrhea.

Study & Design

• Study Type: Intervention
• Study Design: Not specified