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EFFECT OF TENS ON ACUPOINTS IN PREMENSTRUAL SYNDROME

Cairo University (CU) logo

Cairo University (CU)

Status

Unknown

Conditions

Premenstrual Pain

Treatments

Device: Transcutaneous electrical nerve stimulation (TENS)

Study type

Interventional

Funder types

Other

Identifiers

NCT05395156
P.T.REC/012/003688

Details and patient eligibility

About

These will be no effect of transcutaneous electrical acupoint stimulation on premenstrual syndrome Does transcutaneous electrical acupoint stimulation affect premenstrual syndrome (PMS)?

Full description

Premenstrual syndrome is a collection of emotional, physiological, and behavioral symptoms that develop around the end of the luteal phase and fade away with or after menstruation Due to limited evidence on the efficacy of sustained progesterone and the side effects of antidepressant and anxiolytics, in some cases, alternative therapies are recommended for patients with PMS TEAS may be more effective than other forms of transcutaneous electrical nerve stimulation (TENS) in modulating brain activity because acupoint areas contain relatively denser neural and neuroactive components than non-acupoint areas TEAS has been reported to have similar efficacy as acupuncture, electrical acupuncture, and TENS

Enrollment

50 estimated patients

Sex

Female

Ages

18 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Their age will range from 18 to 25 years.
  • The regularity of menstrual cycle is 28-35 days.
  • All of them suffering from moderate and sever PMS.
  • All participants are virgin.
  • Their BMI will range from 25-30 kg\m2.

Exclusion criteria

  • Any pathological findings in the pelvic cavity as PCO, Endometriosis and pelvic inflammatory disease.
  • Any history of gynecological intervention.
  • Have any condition impedes the use of electrotherapy.
  • Receiving sedatives or any medical treatment.
  • Having irregular menstruation.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

sham acupoint
Experimental group
Description:
Control group: (placebo group) will be consisted of twenty-five females diagnosed with premenstrual syndrome. They will receive TEAS on sham acupoint (the acupoint selection site was 1 inch away from the acupoint selection in the study group) daily from 3 days before menstruation to the 4th day of menstruation for 3 consequent menstrual cycles with average of 7 sessions per month for 3 months
Treatment:
Device: Transcutaneous electrical nerve stimulation (TENS)
Electroacupuncture
Experimental group
Description:
Study group: (Electroacupuncture group) will be consisted of twenty-five females diagnosed with premenstrual syndrome. They will receive TEAS on neurogenic acupoints daily from 3 days before menstruation to the 4th day of menstruation for 3 consequent menstrual cycles with average of 7 sessions per month for 3 months.
Treatment:
Device: Transcutaneous electrical nerve stimulation (TENS)

Trial contacts and locations

0

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Central trial contact

Azza Barmoud, professor

Data sourced from clinicaltrials.gov

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