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OpenTrials
Completed

NCT Number: NCT07590232

Acupuncture for Primary Dysmenorrhea

The main aim is to investigate the effects of acupuncture on pain intensity and health-related quality of life in women with primary dysmenorrhea.

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Key information

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Ataturk University Hospital

Erzurum, 25040, Turkey (Türkiye)

About this study

In this randomized controlled clinical trial, 64 women with primary dysmenorrhea were randomly assigned to an acupuncture group (AG; n = 30) or a control group (CG; n = 34). The AG received manual body acupuncture every other day for three menstrual cycles (five sessions per cycle, total of 15 sessions), starting 3-4 days before menstruation in each cycle. The CG received routine recommendations without additional intervention. Pain intensity, functional and emotional impact, and quality of life were assessed using the Visual Analog Scale (VAS), Functional and Emotional Dysmenorrhea Scale (FEDS), and the Short Form-36 (SF-36). Measurements were performed at baseline and on days 30, 60, and 90.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • to be women aged 18-35 years with a confirmed diagnosis of primary dysmenorrhea for at least one year
  • regular menstrual cycles (28 ± 7 days)
  • a VAS score ≥4 in the previous cycle

Exclusion criteria

  • secondary dysmenorrhea
  • currently pregnant, postpartum, or breastfeeding
  • used oral contraceptives or intrauterine devices in the last 3 months,
  • received acupuncture in the past 6 months, had open wounds at acupuncture points
  • presented with severe psychiatric disorder or cognitive impairment

Treatment and study plan

Acupuncture

Other

classical body acupuncture with needle without electrical stimulation

NSAIDs

Drug

NSAID therapy (400 mg ibuprofen three times daily during menstruation) and routine follow-up

Primary outcomes

  1. Visual Analog Scale (VAS)

    Time frame: 3 months

    VAS measures pain severity

Secondary outcomes

  1. The Functional and Emotional Dysmenorrhea Scale (FEDS)

    Time frame: 3 months

    FEDS evaluates the multidimensional impact of dysmenorrhea on participants' daily functioning and emotional well-being

  2. Short Form-36 (SF-36)

    Time frame: 3 months

    SF-36 measures quality of life.

Sponsors and collaborators

Lead sponsor

Ataturk University

Other

Registry information

Official study title

The Effect Of Acupuncture On Pain And Quality Of Life in Primary Dysmenorrhea: A Randomized-Controlled Study

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
May 15, 2026
Registry last updated
May 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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