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Clinical study in the treatment of menstrual cramps

Randomized clinical trial in the treatment of primary dysmenorrhoea syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-67cjv5
Enrollment
Unknown
Registered
2018-07-30
Start date
2018-07-11
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary dysmenorrhoea syndrome

Interventions

Group submitted to transcutaneous electrical nerve stimulation in the anterior pelvic region: 25 women will undergo a 30 minutes care using 4 electrodes in the anterior pelvic region with a frequency
Other
E02.331.800

Sponsors

Centro Universitário de Barra Mansa
Lead Sponsor
Centro Universitário de Barra Mansa
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Accept signing the free and informed consent form; age between eighteen and thirty-five years; pelvic pain caused by primary dysmenorrhea; first to the third day of the menstrual cycle; between one and ten on the analogue visual pain scale

Exclusion criteria

Exclusion criteria: Age less than eighteen and over thirty-five years; patients taking analgesics and other therapies for pelvic pain; gynecological pathologies; undiagnosed abdominal pain; patients with cardiac pacing; cardiac complications; degree 0 on the visual analogue pain scale

Design outcomes

Primary

MeasureTime frame
Reduction of the pain picture verified by the visual analog pain scale by at least 10% in the pre and post-intervention measurements

Secondary

MeasureTime frame
Maintenance of the pain chart determined through the visual analogue pain scale in the post-intervention measurements and two hours after the end of the intervention

Countries

Brazil

Contacts

Public ContactAriela Torres Cruz

Centro Universitário de Barra Mansa

ariela_tcruz@yahoo.com.br+55-024-992192494

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 16, 2026