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Dysmenorrhea clinical trials

View clinical trials related to Dysmenorrhea.

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NCT ID: NCT03561493 Not yet recruiting - Clinical trials for Primary Dysmenorrhea

The Effect of Zumba Dance on Primary Dysmenorrhea

Start date: June 25, 2018
Phase: N/A
Study type: Interventional

the objective of this study is to investigate the effect of practising Zumba exercise in decreasing menstrual pain in young women with primary dysmenorrhea.

NCT ID: NCT03509740 Completed - Dysmenorrhea Clinical Trials

Intravenous Tramadol Versus Intravenous Paracetamol in Patients With Dysmenorrhea

Start date: April 25, 2018
Phase: Phase 4
Study type: Interventional

Patients presented with primary dysmenorrhea composed the study population. One gram paracetamol and 100 mg tramadol in 100 ml saline with a slow infusion were compared in ceasing dysmenorrhea in the emergency department

NCT ID: NCT03448536 Completed - Dysmenorrhea Clinical Trials

A Study to Assess Menstrual Cramp Pain Associated With Primary Dysmenorrhea

Start date: April 5, 2018
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the maximum single dose of Aleve® (two tablets, equivalent to 440 mg of naproxen sodium) to the maximum single dose of Tylenol Extra Strength (two caplets, equivalent to 1000 mg of acetaminophen) in the treatment of menstrual pain associated with primary dysmenorrhea.

NCT ID: NCT03446859 Completed - Clinical trials for Primary Dysmenorrhea

TENS on Pain Intensity in Primary Dysmenorrhea

TENSinPain
Start date: August 4, 2017
Phase: N/A
Study type: Interventional

Dysmenorrhoea is a common problem in women of reproductive age. It is associated with painful uterine contractions and discomfort. The primary aim of the study was to determine the effect of Transcutaneous Electrical Nerve Stimulation (TENS) on pain intensity associated with primary dysmenorrhoea among female undergraduate students of Obafemi Awolowo University. The study involved 50 females undergraduates of Obafemi Awolowo University with primary dysmenorrhoea lasting for at least 5 days. They were allocated in to two groups equally. One group was treated with TENS and other group served as control. The treatment was for 5 days and Pain intensity was measured before and after the treatment in the two groups. The post treatment pain intensity was then compared.

NCT ID: NCT03432611 Recruiting - Clinical trials for Primary Dysmenorrhea

A Smartphone App for Women With Primary Dysmenorrhea

smartAID
Start date: February 19, 2018
Phase: N/A
Study type: Interventional

With a randomized, pragmatic study the effectiveness of a smartphone app for menstrual pain in 18-34-year-old women with primary dysmenorrhea will be investigated.

NCT ID: NCT03421639 Active, not recruiting - Clinical trials for Recurrent Implantation Failure

Aromatase Plus GnRH Analogue Versus GnRH Analog Alone in Adenomyosis

Start date: December 1, 2017
Phase: Phase 4
Study type: Interventional

With this study the investigators want to test which is the best medical treatment for symptomatic adenomyosis affecting women undergoing IVF and with previous implantation failure, between Aromatase inhibitor plus GnRH analog versus GnRH alone, in term pregnancy rate and uterine volume reduction.

NCT ID: NCT03394547 Recruiting - Dysmenorrhea Clinical Trials

Pulsed Electromagnetic Field Treatment for Painful Periods

PUMMP
Start date: November 3, 2017
Phase: N/A
Study type: Interventional

A single-centre, randomised controlled, double blind study comparing use of the Allay pulsed shortwave therapy treatment versus a placebo device or no treatment for management of primary dysmenorrhea.

NCT ID: NCT03325868 Withdrawn - Dysmenorrhea Clinical Trials

Effect of Ulipristal Acetate on Bleeding Patterns and Dysmenorrhea in Women With Adenomyosis

Start date: February 2018
Phase: Phase 4
Study type: Interventional

Adenomyosis affects approximately 21% of symptomatic women who present to gynecology clinics. The disease is characterized by heavy bleeding and pain during periods. Limited treatment options exist for the treatment of adenomyosis for women who desire future child-bearing or prefer to avoid surgery. Recently, ulipristal acetate has been studied as a treatment option for women who have fibroids and heavy bleeding. The majority of women treated with ulipristal stopped having periods altogether. Our study aims to determine whether ulipristal is an adequate treatment for women with adenomyosis.

NCT ID: NCT03323671 Completed - Clinical trials for Primary Dysmenorrhea

Preemptive Analgesia for Primary Dysmenorrhoea

Start date: August 1, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

Preemptive analgesia before the release of pain mediators

NCT ID: NCT03290066 Completed - Clinical trials for Primary Dysmenorrhea

Effectiveness of Kinesiotaping in Primary Dysmenorrhea

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

Determine the effectiveness of kinesiotaping on pain in primary dysmenorrhea.