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Dysmenorrhea clinical trials

View clinical trials related to Dysmenorrhea.

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NCT ID: NCT02255045 Completed - Dysmenorrhea Clinical Trials

Assessment of a Vaginal Ring With Meloxicam in the Treatment of Dysmenorrhea

Start date: June 27, 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The investigators propose that the sustained administration of a vaginal ring would have a better response with respect to pain and a better safety profile than the oral administration of a non-steroidal anti-inflammatory drug. To assess the relief of the symptoms associated with dysmenorrhea, a specific survey was elaborated that also includes a Visual Analog Scale (VAS) to objectify and measure dysmenorrhea as is the case with McGill's Pain Questionnaire (MPQ).

NCT ID: NCT02253446 Completed - Clinical trials for Primary Dysmenorrhea

A Comparison of Analgesic İmpacts of Piroxicam and Diclofenac Sodium in the Treatment of Primary Dysmenorrhea

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

- Currently, nonsteroidal antiinflammatory drugs are widely used by emergency physicians in Turkey for the treatment of patients with Primary Dysmenorrhea. - The objective of the study is compare intramuscular Diclofenac sodium and piroxicam's pain reduction dysmenorrhea in emergency department (ED) adults. - The investigators second aim was to compare recurrent dysmenorrhea pain within 24 hours after discharge.

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: NCT02214550 Completed - Chronic Pain Clinical Trials

Chronic Pain Risk Associated With Menstrual Period Pain

CRAMPP
Start date: July 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if some women with dysmenorrhea (painful periods) are at higher future risk of developing chronic pelvic pain (CPP) and if oral contraceptives (OC) can be used to reverse this chronic pain risk. Investigators will examine whether dysmenorrhea produces CPP via repetitive cross organ sensitization (COS) episodes. The use of cyclical OCs to eliminate dysmenorrhea is expected to reduce COS and decrease the risk of developing CPP.

NCT ID: NCT02205970 Completed - Clinical trials for Primary Dysmenorrhea

Application of Electrical Neurostimulation Transcutaneous in Patients With Primary Dysmenorrhea.

Start date: August 2010
Phase: N/A
Study type: Interventional

The present study aims to verify the analgesic potential of a new methodological proposal for application for transcutaneous electrical nerve stimulation (TENS interactive) using patients with primary dysmenorrhoea and compare it with placebo in a randomized double blind study with convenience sample.

NCT ID: NCT02197936 Terminated - Infertility Clinical Trials

Norwegian Adenomyosis Study III: Peristalsis

NAPPEDIII
Start date: July 2014
Phase:
Study type: Observational

Spontaneous contractions (peristalsis) of the non-pregnant uterus is widely investigated and the role of correct peristalsis is most important for correct sperm transport towards the fallopian tubes and implantation of the embryo, thus obtaining pregnancy. At the same time, an impaired uterine peristalsis is discussed to be the reason for lower pregnancy rates and may also account for heavy menstrual bleedings and menstrual pain. In this study, the uterine peristalsis of women with adenomyosis will be investigated. This condition is associated to heavy menstrual bleeding, menstrual pain and infertility.

NCT ID: NCT02183025 Completed - Dysmenorrhea Clinical Trials

Efficacy and Safety Study of Meloxicam Versus Mefenamic Acid in Patients With Dysmenorrhea

Start date: January 1998
Phase: Phase 2
Study type: Interventional

To access the efficacy and safety of Meloxicam 7.5 mg and 15 mg once daily compared with Mefenamic acid 500 mg t.i.d. over a treatment period of 3-5 days, during an observation period of 3 menstrual cycles, for the symptomatic relief of primary dysmenorrhea

NCT ID: NCT02114723 Completed - Clinical trials for Primary Dysmenorrhea

Effectiveness of Medical Taping Concept in Primary Dysmenorrhea

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

Determine the effectiveness of a proceeding under kinesio tape on pain and systemic symptoms most frequently described in primary dysmenorrhea.

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: NCT02026206 Completed - Clinical trials for Primary Dysmenorrhea

Low-level Light Therapy for Primary Dysmenorrhea

Start date: October 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study was to evaluate the effectiveness of a self-therapeutic approach of skin adhesive low-level light therapy (LLLT) in females with primary dysmenorrhea (PD).