Clinical Trials Logo

Dysmenorrhea clinical trials

View clinical trials related to Dysmenorrhea.

Filter by:

NCT ID: NCT02602522 Completed - Clinical trials for Primary Dysmenorrhea

Danshen-Jiang-Fu Granule Prepared by Danshen From Different Producing Areas for Primary Dysmenorrhea

Start date: November 2015
Phase: Early Phase 1
Study type: Interventional

This trial aims to compare the effect of Danshen-Jiang-Fu Granule prepared by Danshen (Salvia Miltiorrhiza) from different producing areas (Shandong and Sichuan) for the relief of primary dysmenorrhea.

NCT ID: NCT02539706 Completed - Pain, Menstrual Clinical Trials

Menstrual Cycle on Injection Pain of Rocuronium

MENS
Start date: January 6, 2014
Phase: N/A
Study type: Interventional

This study evaluates the effects of rocuronium injection pain to menstrual cycle phases.Half of participants will receive follicular phase, while the other half will receive luteal phase.

NCT ID: NCT02475356 Completed - Clinical trials for Menorrhagia, Dysmenorrhea

Prospective, Non-interventional, Multi-center Safety Study of Mirena for Heavy Menstrual Bleeding and Dysmenorrhea

J-MIRAI
Start date: August 4, 2015
Phase:
Study type: Observational

The primary objective in this study is collecting post-marketing information on the safety. Thus, it includes information under the routine clinical practice on adverse events (AEs) and adverse drug reactions (ADRs) including expulsion and abnormal bleeding that occur within the first 12 months Mirena insertion. The secondary objective(s) in this study is/are collecting information on Mirena effectiveness, such as periodic blood loss and Quality of life (QOL), use of analgesic and dysmenorrhea pain as far as these are recorded under routine clinical practice.

NCT ID: NCT02467543 Completed - Dysmenorrhea Clinical Trials

The Efficacy of Viburnum Opulus 3X in the Treatment of Primary Dysmenorrhea

Start date: February 2015
Phase: Phase 2
Study type: Interventional

Dysmenorrhea (painful menstruation) is a common gynaecological disorder that is prevalent in more than 50% of women during their reproductive years. Primary dysmenorrhea describes cyclic uterine pain without any identifiable or underlying causes. Menstrual pain results as a consequence of endometrial ischemia, high levels of prostaglandins and other inflammatory mediators. Conventional treatment for primary dysmenorrhea consists of non-steroidal anti-inflammatory drugs and oral contraceptives, which may have adverse effects. Viburnum opulus (Cramp bark) is a homoeopathic remedy well indicated for the treatment of dysmenorrhea. While there are studies using Viburnum opulus in its herbal form, there is no research assessing its efficacy in the homoeopathic form. The aim of this study is to determine the efficacy of Viburnum opulus 3X in the treatment of primary dysmenorrhea as measured with the modified Short Form McGill pain questionnaire (SF-MPQ-2) and visual analogue scale (VAS) respectively.

NCT ID: NCT02441530 Completed - Clinical trials for Primary Dysmenorrhoea

Effectiveness of Vitamin D in Primary Dysmenorrhoea

Start date: November 2012
Phase: Phase 3
Study type: Interventional

Vitamin D in the treatment of primary dysmenorrhoea. Design:Randomised controlled trial. Setting:In a university hospital. Population: 142 women aged 16-35 years. Methods: Patients were treated with 667 unit of vitamin D once a day, 200 unit of vitamin E once a day or 400 mg ibuprofen twice a day,2 days before the date of menstruation and continued through the first 3 days, for 2 months. Main outcome measures: Pain score. Results: Mean VAS of vitamin D group was 4,91, was 6,54 in the vitamin E group and was 4,02 in the ibuprofen group Conclusion:Vitamin D and vitamin E are effective in relieving the pain,but the effect of vitamin D are more prominent

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: NCT02372123 Completed - Pelvic Pain Clinical Trials

The Effect of Connective Tissue Massage in Women With Primary Dysmenorrhoea

Start date: February 2015
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the effect of connective tissue manipulation on pain threshold in women with primary dysmenorrhoea. According to literature, there are studies that measure the pain threshold. But there is no randomized controlled trial which explore the short and long-term effects of connective tissue manipulation on primary dysmenorrhoea. Hypothesis of this study is that connective tissue manipulation increases pain threshold and decreases severity of pain in women suffer with primary dysmenorrhoea.

NCT ID: NCT02362711 Completed - Dysmenorrhea Clinical Trials

Efficacy and Safety, Long-Term Study of NPC-16 to Treat Dysmenorrhea

Start date: February 2015
Phase: Phase 3
Study type: Interventional

The purpose of this long-term study is to determine whether NPC-16 is effective in the treatment of dysmenorrhea.

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: NCT02274714 Completed - Ulcerative Colitis Clinical Trials

Dysmenorrhea in Women With Crohn's Disease and Ulcerative Colitis

Start date: May 2010
Phase: N/A
Study type: Observational

This case-control study will screen for dysmenorrhea and assess severity of menstrual symptoms in menstruating women with CD and UC compared with healthy age-matched controls. IBD activity will be characterized using previously validated clinical disease activity indices. General and health-related quality of life will be assessed using validated measures.