Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
FEMALE
NCT07248540

IV Magnesium in the Treatment of Acute Dysmenorrhea

Led by Havva Betül Bacak · Updated on 2025-11-25

60

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This prospective, randomized, double-blind clinical trial aims to evaluate the analgesic efficacy of intravenous magnesium sulfate in women presenting to the emergency department with acute dysmenorrhea. Participants will be randomized into two groups receiving either 2 ampoules of magnesium sulfate or intravenous dexketoprofen. Pain levels will be assessed using the Visual Analog Scale (VAS) before and after treatment.

CONDITIONS

Official Title

IV Magnesium in the Treatment of Acute Dysmenorrhea

Who Can Participate

Age: 18Years - 35Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female patients aged 18 to 35 years
  • Presenting to the obstetrics and gynecology emergency department with a diagnosis of primary dysmenorrhea
  • Having regular menstrual cycles within the last 6 months
  • Having a Visual Analog Scale (VAS) pain score of 6 at emergency admission
  • Providing written informed consent for participation in the study
Not Eligible

You will not qualify if you...

  • Patients with secondary dysmenorrhea or underlying gynecological pathology
  • Pregnancy or breastfeeding
  • Use of analgesics or muscle relaxants within the last 3 days
  • Known allergy to magnesium sulfate or dexketoprofen trometamol
  • History of renal failure, cardiac arrhythmia, or serious systemic disease
  • Inability to assess pain due to mental disability or communication disorder
  • Failure to provide informed consent for participation in the study

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

SBÜ Gaziosmanpaşa Training and Research Hospital

Gaziosmanpaşa, Outside of the US, Turkey (Türkiye), 33400

Actively Recruiting

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Research Team

E

ecenur çelikoğlu, md

CONTACT

Y

yağmur acıyiyen, md

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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