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Premenstrual Syndrome clinical trials

View clinical trials related to Premenstrual Syndrome.

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NCT ID: NCT04955912 Completed - Clinical trials for Premenstrual Syndrome

Music and Premenstrual Symptoms and Quality of Life

Start date: January 30, 2021
Phase: N/A
Study type: Interventional

Premenstrual syndrome is an important health problem affecting women of childbearing age. This study is a prospective, single-blinded randomized controlled trial. Participants were randomized into music, and control groups. Immediately post-intervention, the women in the experimental groups had significantly higher reduce premenstraul syndrome levels and increase a quality life.

NCT ID: NCT04901598 Completed - Clinical trials for Premenstrual Syndrome

Physical Activity Level, Aerobic Capacity and Dietary Habits Among a Cohort of Females With Premenstrual Syndrome

Start date: October 20, 2021
Phase:
Study type: Observational

The aim of the study is to investigate the physical activity level, aerobic capacity and dietary habits among a cohort of females with premenstrual syndrome

NCT ID: NCT04855981 Completed - Clinical trials for Premenstrual Syndrome

Whole-body Vibration Versus Aerobic Exercise on the Inflammatory Status and Hormonal Parameters Premenstrual Syndrome

PMS
Start date: April 15, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate and compare the effect of whole-body vibration to aerobic exercise on inflammatory status in females with premenstrual syndrome.

NCT ID: NCT04838691 Completed - Clinical trials for Premenstrual Syndrome

Premenstrual Syndrome and Interpersonal Counseling

Start date: April 6, 2020
Phase: N/A
Study type: Interventional

This study aims to test the effectiveness of interpersonal counseling in PMS symptom management in university students experiencing PMS symptoms.

NCT ID: NCT04618172 Completed - Clinical trials for Premenstrual Syndrome

Effects of Exercise on the Symptoms of Premenstrual Syndrome and Dysmenorrhoea and Blood Flow of Genital Tract

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

Effects of exercise on the symptoms of premenstrual syndrome and dysmenorrhoea and blood flow of genital tract. Different self-reported questionnaires and vaginal ultrasound flowmetry are used in the prospective observational trial. The study has interventional and control groups. There are changes in premenstrual syndrome complaints and dysmenorrhoea complaints during the study period.The deegre of menstrual pain and self-awareness improve during the period of study. The ultrasound examination shows changes in genital blood flow after exercise.

NCT ID: NCT04600388 Completed - Menstrual Migraine Clinical Trials

Efficacy and Safety of Nerivio for the Acute Treatment of Menstrual Migraine

Start date: September 9, 2020
Phase:
Study type: Observational

Post-marketing, retrospective, observational survey study. Users (menstruating women only) of Nerivio who have used Nerivio at least 4 times between October 2019 and December 2020 will be contacted by email and/or through an app notification and will be asked to complete a 5-minute online anonymous survey assessing satisfaction, effectiveness, and safety. Eligible users will sign an informed consent form (the consent language will appear as the first page of the survey, and participants will click either "agree" or "disagree" to the consent statement; those who click "agree" will proceed to the survey, those who click "disagree" will be brought to an exit page) and complete a survey asking about their satisfaction with Nerivio and the effectiveness and safety of the device for acute treatment of menstrual migraine. During the survey, participants will be screened to verify that they have menstrual migraine (self-reported) and have used Nerivio to treat menstrual migraines.

NCT ID: NCT04455685 Completed - Clinical trials for Premenstrual Syndrome

Prevalence of Self-reported Premenstrual Syndrome and Analysis of Somatic and Psychoemotional Symptoms

LB2007
Start date: June 29, 2020
Phase:
Study type: Observational

In Brazil there are few published studies that study, the prevalence, symptoms and the population's knowledge about the premenstrual syndrome of women of reproductive age, and that correlate these data with the sociodemographic conditions of these women. In addition, given the complexity of the diagnosis of PMS, the prevalence of PMS in the Brazilian female population may be lower than the self-reported and published in these works, since not all women who believe they suffer from PMS fully comply with the criteria contemplated in the consensus for diagnosis of PMS. In this sense, this study aims to analyze the prevalence and intensity of frequent symptoms of PMS reported by the Brazilian female population. The information generated with this study may help to rethink behaviors to improve the health and quality of life of these women, as well as offer tools for decision making related to the need for early and effective treatment of PMS, whose disorders are associated with both the fall present and future quality of life for women, as well as all of their family, social and professional coexistence.

NCT ID: NCT04348201 Completed - Clinical trials for Dietary Modification

Foot Reflexology on Premenstrual Syndrome

Start date: June 24, 2010
Phase: N/A
Study type: Interventional

: Premenstrual Syndrome (PMS) is a set of physical, emotional and behavioral symptom that start during the week preceding menstruation and are alleviated when the menstrual flow begins. Reflexology is one of the most popular complementary therapies

NCT ID: NCT04320641 Completed - Nursing Caries Clinical Trials

The Effect of Acupressure and Yoga on Premenstrual Symptoms and Quality of Life

Start date: February 15, 2019
Phase: N/A
Study type: Interventional

The research was carried out to determine the effect of acupressure and yoga applied to cope with PMS on premenstrual symptoms and quality of life.

NCT ID: NCT04102995 Completed - Menstrual Migraine Clinical Trials

A Study Investigating the Efficacy and Safety of Sepranolone in Women With Menstrual Migraine

APH204
Start date: August 27, 2019
Phase: Phase 2
Study type: Interventional

The objective of this phase 2 Proof.of Concept study is to evaluate the efficacy and safety of Sepranolone (UC1010) in preventing menstrual migraine attacks in adult women with migraine occurring between Day -2 and Day 5 of the menstrual cycle. Patients will be taking Sepranolone or Placebo (blinded to patient and study doctor) during the two week preceding the menstruation for three menstrual cycles. Effect (change from baseline) will be assessed by comparison of symptoms recorded daily by the patients using an electronic diary using validated scales for assessment of menstual migraine symptoms. Sepranolone is identical to an endogenous steroid.