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Impacts of Static Magnetic Fields on Dysmenorrhea Pain

Nova Southeastern University (NSU) logo

Nova Southeastern University (NSU)

Status

Completed

Conditions

Period Pain

Treatments

Device: Magnet

Study type

Interventional

Funder types

Other

Identifiers

NCT04539691
2018-614-NSU

Details and patient eligibility

About

Study to determine the effectiveness of a certain type of magnet to reduce period pain

Full description

Young women with their period pain levels of 6 or greater on a pain scale of 0-10 will wear a concentric magnet or a sham that is positioned close to the maximum pain site. The pain score after wearing either the magnet or sham will be recorded.

Enrollment

60 patients

Sex

Female

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: Female with period pain score consistently equal to or greater than 6 on a pain scale of 0-10 -

Exclusion Criteria:

  1. Pain not experienced on almost all menstrual cycles
  2. Having secondary dysmenorrhea including endometriosis, fibroids or pelvic inflammatory disease
  3. Having a pacemaker or any implanted wires or devices -

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Magnet group
Experimental group
Description:
Women wearing magnet a magnet, or sham device indistinguishable from the magnet (determined randomly), will be placed on her abdomen. If the pain is predominately in her abdomen, the device will be placed on the location with the most pain. If the pain is predominantly in the subjects back, the device will be placed on the lower abdomen on the midline between the umbilicus and the pubic bone.
Treatment:
Device: Magnet
Sham group
Sham Comparator group
Description:
Women wearing sham a magnet, or sham device indistinguishable from the magnet (determined randomly), will be placed on her abdomen. If the pain is predominately in her abdomen, the device will be placed on the location with the most pain. If the pain is predominantly in the subjects back, the device will be placed on the lower abdomen on the midline between the umbilicus and the pubic bone.
Treatment:
Device: Magnet

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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