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Dysmenorrhea clinical trials

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NCT ID: NCT02685501 Recruiting - Clinical trials for Iron Deficiency Anemia

Menorrhagia, Dysmenorrhea and Iron Deficiency Among Young Women Soldiers and Effect on Activity

Start date: January 2016
Phase: N/A
Study type: Observational

As combat women soldiers are required to more intensive daily activity the investigators believe that the impact of menorrhagia, dysmenorrhea and its clinical consequence (as characterized by, anemia iron deficiency and reduced quality of life)) on personal performance will be more significant in combat women soldiers compared to non-combat women soldiers. Using cohorts from the same environment will enable the investigators to better study the effect of menorrhagia and dysmenorrhea eliminating other uncontrolled factors, such as nutrition. The study does not include any intervention.

NCT ID: NCT02373514 Recruiting - Dysmenorrhea Clinical Trials

IV Paracetamol Versus IV Dexketoprofen in Dysmenorrhea

Start date: January 2015
Phase: Phase 4
Study type: Interventional

Patients presented with dysmenorrhea composed the study population. One gram paracetamol and 50 mg dexketoprofen in 100 ml saline with a rapid infusion were compared in ceasing dysmenorrhea in emergency department.

NCT ID: NCT02301559 Recruiting - Pain Clinical Trials

The Influence of the Method Pilates in Women With Primary Dysmenorrhea

Start date: September 2014
Phase: N/A
Study type: Interventional

Primary dysmenorrhea is the result of hypercontractility and uterine vascular ischemia is the most common gynecologic complaints in young women. According to the intensity of symptoms may impair daily living, work and leisure activities. Pilates brings the concept of moving the body for the recovery, maintenance and promotion of health through exercises that stimulate circulation, improving physical conditioning, flexibility and proper postural alignment, and promote improvement in the levels of body awareness, coordination and muscle control. In this sense, the objective is to investigate the effects of pilates in the symptomatology of primary dysmenorrhea. This is a study to be developed with students of Physical Therapy from the State University of Piauí-UESPI presenting with primary dysmenorrhea compatible clinical picture. A questionnaire will be used for research. The students with the framework of dysmenorrhea that meet the inclusion criteria will be assessed for anthropometric parameters, pain, flexibility, indirect assessment of contraction of transversus abdominis and quality of life before and after the treatment protocol using the pilates method, often 3 weekly meetings, totaling 20 sessions.

NCT ID: NCT02237131 Recruiting - Pelvic Pain Clinical Trials

Continuous Versus Cyclic Oral Contraceptives for Endometriosis

Start date: April 2014
Phase: Phase 4
Study type: Interventional

To evaluate the efficacy of oral contraceptives in a continuous fashion versus the usual cyclic fashion in the recurrence of endometriosis related symptoms and endometriomas following fertility-sparing surgery.

NCT ID: NCT02031523 Recruiting - Dysmenorrhea Clinical Trials

Multi-center Clinical Trials of Sanjie Analgesic Capsule in Treating Endometriosis

Start date: October 2013
Phase: Phase 4
Study type: Interventional

It is a multi-center, double -blind, placebo -controlled, randomized post-marketing study in Chinese subjects with endometriosis-associated pain to assess treatment effect and safety in the subjects treated with Sanjie Analgesic Capsule versus subjects treated with placebo.

NCT ID: NCT01289314 Recruiting - Dysmenorrhea Clinical Trials

Long Term Outcomes Following Total Laparoscopic Hysterectomy and Laparoscopic Supracervical Hysterectomy

Start date: February 2011
Phase: N/A
Study type: Interventional

Objective: To compare the occurrence and intensity of pelvic pain as well as patient satisfaction and quality of life after total laparoscopic and laparoscopic supracervical hysterectomy. Design: Prospective randomised trial. Null hypothesis 1: There is no significant difference in occurrence and intensity of pelvic pain following TLH compared with following LSH. Null hypothesis 2: There is no significant difference in patient satisfaction and quality of life following TLH compared with following LSH.

NCT ID: NCT00740818 Recruiting - Clinical trials for Menstrual Distress (Dysmenorrhea)

Logan Basic and Dysmenorrhea

Start date: July 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effects of Logan Basic Technique on symptoms of dysmenorrhea.

NCT ID: NCT00689897 Recruiting - Clinical trials for Primary Dysmenorrhea

Psychological Outcomes From a Study of Acupuncture Treatment on Experimentally Primary Dysmenorrhea

Start date: June 2008
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the associations between deqi, the effects of acupuncture and personality in primary dysmenorrhea and to characterize the nature of the deqi phenomenon on terms of the prevalence of sensations as well as the uniqueness of the sensations underlying the deqi experiment.