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Mastodynia clinical trials

View clinical trials related to Mastodynia.

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NCT ID: NCT03715413 Completed - Breast Fibroadenoma Clinical Trials

Analgesic Efficacy of Pulsed Radiofrequency in Non-cyclic Mastalgia

Start date: August 15, 2018
Phase: Phase 2
Study type: Interventional

Background: Breast pain, mastalgia or mastodynia, is recognized as an organic benign breast disease. Mastalgia may be bilateral, may be in only one breast or part of one breast, and may radiate to the axilla and down the medial aspect of the upper arm. This study aimed to evaluate the additional pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia to the routine regimen treatment of mastalgia tamoxifen 10 mg daily may improve breast pain severity and quality of life. Method: Patients was randomly classified into two groups:Group A (n=13): they was received Tamoxifen 10 mg daily. Group B (n=13): they was received Tamoxifen 10 mg daily and pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia. The following parameters were monitored: Primary outcome: VAS after injection and at interval two weeks, 1, 2 and 3 months after injection. Secondary outcome:1-Immediate complications for ex. Hematoma, neurological deficits or respiratory insufficiency (dyspnea or pneumothorax).2-Need for analgesic intake was recorded.3-Side effect of Tamoxifen as nausea, vomiting, hot flashes and dizziness.4-Quality of life (The American Chronic Pain Association's Quality of life scale).

NCT ID: NCT03392675 Completed - Breastfeeding Clinical Trials

Breastfeeding Self-Management for Nipple and Breast Pain

BSM
Start date: April 24, 2017
Phase: N/A
Study type: Interventional

This pilot project will provide an understanding of the contextual variables responsible for breast and nipple pain during breastfeeding initiation. These variables include, genetic variation, pain sensitivity, reactivity, pain catastrophizing and perceived stress. The purpose is to understand the efficacy of self-management (SM) strategies on each of these contextual variables, in an effort to inform a personalized approach to managing breastfeeding pain and its effect on improved health outcomes.

NCT ID: NCT03084536 Completed - Breast Cancer Clinical Trials

PECS Block vs. Multimodal Analgesia for Prevention of Persistent Postoperative Pain in Breast Surgery

Start date: June 7, 2017
Phase: Phase 2
Study type: Interventional

In this double blinded randomized placebo-controlled trial, 160 subjects scheduled for breast surgery involving the axilla will be administered a multimodal pain regimen including acetaminophen, dexamethasone, celecoxib, and gabapentin. 80 subjects will also receive a Pectoral Nerve blocks I and II (PECS I and II block) preoperatively.

NCT ID: NCT02848989 Completed - Breast Cancer Clinical Trials

Qigong For PPSP In Breast Cancer Pain In Breast Cancer Survivors

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

Studies have shown that on-going pain following breast surgery is common and may limit the ability to participate in physical activity, cause tiredness, difficulty in daily chores/activities as well as other problems. This study is evaluating whether participating in a 12-week Qigong program (pronounced chee kung), an exercise program that involves gentle movements combined with breathing/relaxation techniques, also known as mind-body exercise, leads to improvement of pain, physical function, and quality of life among breast cancer survivors that have significant pain following surgery.

NCT ID: NCT02810236 Completed - Anxiety Clinical Trials

Focal Breast Pain: Does a Normal Ultrasound Provide Reassurance?

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

The investigator hypothesizes that a benign directed ultrasound, when performed after a normal digital mammogram, will provide women with focal breast pain additional reassurance that the etiology of their symptom is benign. 160 women over the age of thirty with focal breast pain who present to the Breast Imaging Clinic for evaluation between 3/1/2016 - 7/1/2018 will be selected and randomized to three groups using a block randomization technique. All study participants will complete a survey assessing psychosocial factors, then receive a digital mammogram. Patients with a negative mammogram will continue on with the study and will either have a conversation about their negative mammogram with a radiologist or receive a directed ultrasound. A second survey will be conducted assessing psychosocial factors. All study participants who did not receive an ultrasound will receive an ultrasound so that all study participants are provided with the standard of care for focal breast pain. The results of the survey will be compared and appropriate statistical analyses such as an Analysis of Variance (ANOVA) test will be conducted to determine any statistically significant differences between the three randomized groups. The risks/safety issues of this study are believed to be minimal.

NCT ID: NCT02784379 Completed - Mastalgia Clinical Trials

Electromyography of the Pectoral Muscle in Mastalgia Patients

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

Mastalgia is a common problem for women. The aim of this study is to investigate the role of neuromuscular pathologies of the thorax wall at mastalgia ethiopathogenesis.

NCT ID: NCT02515253 Completed - Mastodynia Clinical Trials

A Breast Support Intervention for Women With Breast Pain

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

The purpose of this study is to assess whether prescribing a bra to participants results in an improvement in the Patient Global Impression of Change (PGIC) compared to participants who receive standard care alone.

NCT ID: NCT02093338 Completed - Breast Pain Clinical Trials

L.Fermentum CECT5716 in Treatment of Breast Pain

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

The main objective of this intervention study is to evaluate the efficacy of Lactobacillus fermentum CECT5716 to reduce the presence in the milk of genera Staphylococcus and Streptococcus as risk factors for mastitis in women with breast pain

NCT ID: NCT01752907 Completed - Breast Cancer Clinical Trials

Effect of Patient Education on Reported Bone Pain in Breast Cancer Patients Receiving Chemotherapy and Pegfilgrastim

VINE
Start date: January 17, 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if patient education can affect patient reported bone pain in breast cancer patients receiving chemotherapy and pegfilgrastim.

NCT ID: NCT01639417 Completed - Breast Cancer Clinical Trials

Pilot Functional Imaging Study to Evaluate Mechanisms Underlying Chronic Pain in Breast Cancer Patients

Start date: May 2012
Phase: N/A
Study type: Observational

The purpose of this study is to better understand why some women with breast cancer develop chronic pain.