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Chronic Pelvic Pain clinical trials

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NCT ID: NCT03590236 Active, not recruiting - Chronic Pelvic Pain Clinical Trials

Graded Exposure Therapy in Chronic Pelvic Pain

Start date: August 20, 2017
Phase: N/A
Study type: Interventional

Chronic pelvic pain (CPP) is considered as nonmalignant recurrent or continuous pain related to the structures of the pelvis. The objective of this study was to evaluate the effects of graded exposure therapy in women with chronic pelvic pain.

NCT ID: NCT03541954 Terminated - Chronic Pelvic Pain Clinical Trials

Neurophysiological Validation of the Clinical Criteria of Sensitization in Chronic Pelvic and Perineal Pain Population

DOPEC
Start date: July 17, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to assess and validate the clinical criteria of sensitization ("Convergences PP criteria") selected by the expert consensus with neurophysiological sensory testing.

NCT ID: NCT03272360 Withdrawn - Endometriosis Clinical Trials

Endometriosis Biomarker Discovery Study

EMBARK
Start date: September 2016
Phase: N/A
Study type: Observational

This is a prospective, Single time point, discovery study intending to identify biomarkers that can differentiate endometriosis from other underlying reasons for pelvic pain. Patients undergoing laparoscopy for evaluation of chronic pelvic pain or elective tubal ligation will be enrolled for collection of tissue samples at the time of laparoscopy.

NCT ID: NCT03251560 Recruiting - Chronic Pelvic Pain Clinical Trials

The Clinical Effect of Fuke Qianjin Capsule on Chronic Pelvic Pain Caused by Pelvic Inflammation

Start date: December 1, 2016
Phase: Phase 2
Study type: Interventional

A prospective random control clinical trials to research Fuke Qianjin capsule's effects on ameliorating the pain caused by chronic pelvic disease.

NCT ID: NCT03204682 Recruiting - Chronic Pelvic Pain Clinical Trials

Repetitive Transcranial Magnetic Stimulation as an Analgesic Treatment in Endometriosis Chronic Pain : Feasibility

ENDOSTIM
Start date: April 13, 2016
Phase: N/A
Study type: Interventional

Endometriosis is associated with different types of pain (acute, chronic, excess nociception, neuropathic) generated by different mechanisms in the nervous system. The rTMS could provide significant analgesia for refractory endometriosis pain. The aim of the study is to evaluate the feasibility of transcranial magnetic stimulation (rTMS) for analgesia on chronic refractory endometriosis pain.

NCT ID: NCT03175809 Completed - Chronic Pelvic Pain Clinical Trials

Pelvic Floor Muscles Training Associated Dry Needling for Chronic Pelvic Pain

Start date: June 9, 2017
Phase: N/A
Study type: Interventional

The presence of trigger points in the pelvic floor musculature (PFM) is a frequent condition in individuals with chronic pelvic pain (CPP) and is associated with higher levels of pain, disability and functional decline. The purpose of this study is to test the effectiveness of two interventions: pelvic floor muscle (PFM) training with biofeedback and PFM training with the addition of trigger point dry needling applied over(Lumbar square, psoas, external obliques, gluteus medius, piriformis and adductors) on pain and quality of life of women with CPP.

NCT ID: NCT02721108 Completed - Chronic Pelvic Pain Clinical Trials

Mindfulness Meditation for Chronic Pelvic Pain Management

MEMPHIS
Start date: May 2016
Phase: N/A
Study type: Interventional

Chronic pelvic pain (CPP) in women is common, painful and disabling and puts much strain on women's lives and the (National Health Service) NHS. CPP may be related to internal organs, the nervous system or psychological factors and is often difficult to treat. Surgery and drugs have risks and side effects, are expensive and do not help all patients. Psychological treatments have potential to improve CPP but are not consistently available. Mindfulness meditation teaches people to accept their sensations and emotions in the present moment. This can help to accept pain better, which enables patients to focus on daily activities and improve their quality of life. It has been shown to help in headache, back pain and depression. Usually mindfulness meditation is taught by attending courses for 8 weeks. The investigators want to find out in a full-scale trial if mindfulness meditation, taught by using a smartphone app, can help CPP patients. In preparation for this full-scale study the investigators will conduct the MEMPHIS study to answer the following questions: - How many patients are willing to participate? - How often they use the app? - Reasons for not wanting to participate/not using the app - - Which health questionnaires are the most useful ones? - How many patients will be required for the full-scale trial? Patients will receive the usual treatment and be divided into three groups - using a 60-day mindfulness meditation app, -- using comparison app with progressive muscle relaxation but no meditation - no app Patients will complete health questionnaires, may be asked to comment in a focus group and record pain, medication changes, surgery and emergency medical visits

NCT ID: NCT02556411 Not yet recruiting - Adenomyosis Clinical Trials

Comparison of Estrogen-progestin Therapy in Continuous Regimen Versus Combination Estrogen-progestin Therapy in Continuous Regimen Plus Levonorgestrel-releasing Intrauterine System (LNG-IUS)

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

Adenomyosis is characterized by the appearance of endometrial cells in the muscular layer of the uterus. It affects about 15-20% of the female population. The symptoms of adenomyosis are heavy menstrual bleedings and painful menstruation (dysmenorrhea) and in addition chronic pelvic pain. Regarding treatment levonogestrel-releasing intrauterine system, Gonadotropin releasing hormone (GnRH)-analogues, Danazol, uterine embolization and endometrial ablation have been tried. The aim of this study is to compare the efficacy and usefulness of association of oral contraceptive pill and LNG-IUS or LNG-IUS alone

NCT ID: NCT02472587 Active, not recruiting - Chronic Pelvic Pain Clinical Trials

Assessing Chronic Pain Conditions in General Population

Start date: January 2013
Phase: N/A
Study type: Observational

The purpose of this study is to determine the percentage of women, among those attending our institute in order to do Pap test, suffering of chronic pelvic pain. To such purpose the patients will be submitted to questionnaires.

NCT ID: NCT02372903 Completed - Endometriosis Clinical Trials

Efficacy of Palmitoylethanolamide-polydatin Combination on Chronic Pelvic Pain in Patients With Endometriosis

Start date: October 2013
Phase: N/A
Study type: Interventional

One of the main symptoms of endometriosis is pain, but his pathogenesis is not fully understood. The detection of mast cells in the endometriosis lesions supports the hypothesis that mast cell degranulation may contribute to development of pain and hyperalgesia. N-acylethanolamines (NAEs) are a class of endogenous compounds that regulate inflammation and pain, controlling mast-cell activation. The aim of the study is to investigate the efficacy of palmitoylethanolamide-polydatin combination on pain relief in symptomatic patients with endometriosis.