Clinical Trials for Pelvic Pain

Currently registered clinical trials for Pelvic Pain from ClinicalTrials.gov. 15 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Pelvic Pain from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 15
  • Active, not recruiting: 4
  • Completed: 11
  • Other: 20

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT00499317 — Genetic Study of Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS)

StatusRecruiting
PhaseN/A
SponsorBoston Children’s Hospital
Enrollment500
Study TypeOBSERVATIONAL
ConditionsChronic Prostatitis (CP); Chronic Pelvic Pain Syndrome (CPPS); Painful Bladder Syndrome (PBS); Benign Frequency Syndrome (BFS); Interstitial Cystitis

Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS) is a condition with several causes of which some remain unknown. It is believed that some types of CP may be genetic or passed down (inherited) from one generation to the next.

In this study, we are collecting genetic material and medical information to try to determine if genetic factors play a role in CP/CPPS. We will be collecting D…

NCT05245695 — Deep Neural Network Stratification for Use Detecting Endometriosis in Women Affected by Chronic Pelvic Pain (EndoCheck)

StatusRecruiting
PhaseN/A
SponsorAspira Women’s Health
Enrollment1200
Study TypeOBSERVATIONAL
ConditionsEndometriosis
Interventions

The goal of this observational study is to determine the clinical validity of a deep neural network algorithm that utilizes protein biomarker detection of Endometriosis - “EndoCheck” - as an “aid in diagnosis” for endometriosis and to show validity as a diagnostic test

StatusRecruiting
PhaseN/A
SponsorYI-JU TSAI
Enrollment60
Study TypeINTERVENTIONAL
ConditionsPostpartum; Pregnancy Related; Pelvic Girdle Pain
Interventions; ;

The goal of this interventional study is to compare investigate the short-term and long-term effects of 8-week real-time telehealth-based diaphragmatic breathing exercise and pelvic stabilization exercise on pain, disability, and quality of life in postpartum women with pregnancy-related pelvic girdle pain.

NCT07440849 — Effects of Core Stability and Pelvic Clock Exercises in Sacroiliac Joint Dysfunction

StatusRecruiting
PhaseN/A
SponsorRiphah International University
Enrollment50
Study TypeINTERVENTIONAL
ConditionsSacroiliac Joint Dysfunction
Interventions;

The study will be a randomized control trial and will be conducted in DHQ and Sadiq Hospital in Sargodha District. This study will be completed in time duration of 10 months after the approval of synopsis. Nonprobability convenience sampling technique will be used and 50 participants will be recruited in study after randomization. The subjects will be divided into two groups. Group A(Experiment…

NCT06955221 — Effect of Alcohol Sclerotherapy on Pelvic Pain and Quality of Life in Women With Ovarian Endometriosis

StatusRecruiting
PhaseN/A
SponsorHospital Universitari de Bellvitge
Enrollment288
Study TypeINTERVENTIONAL
ConditionsEndometrioma; Ultrasound Therapy; Complications; Quality of Life; Pelvic Pain
Interventions

The goal of this clinical trial is to evaluate whether ultrasound-guided alcohol sclerotherapy can improve pelvic pain and quality of life in women aged 18 to 45 diagnosed with ovarian endometriomas, compared to expectant management.

The main questions it aims to answer are:

  1. - Does sclerotherapy significantly reduce pelvic pain compared to expectant management?
  2. - Does sclerotherapy im…

NCT06796985 — Botox for Chronic Pelvic Pain

StatusRecruiting
PhasePhase 1
SponsorUniversity of Miami
Enrollment30
Study TypeINTERVENTIONAL
ConditionsPelvic Floor Disorders
Interventions;

The purpose of this research study is to find out if precise, targeted injection of botulinum neurotoxin (commonly known as Botox) provides better relief of pelvic floor hypertonicity and pain than the standard method being used. The researchers want to better understand the effects (good and bad) of targeted botulinum neurotoxin injections in women with pelvic floor disorders.

NCT07642180 — Combined Effects of Pelvic Floor Retraining and Hypopressive Exercises in Uterine Prolapse Outcomes

StatusRecruiting
PhaseN/A
SponsorRiphah International University
Enrollment32
Study TypeINTERVENTIONAL
ConditionsUterine Prolapse
Interventions;

One common pelvic floor condition, particularly in postpartum or later life, is uterine prolapse. It is caused by weak pelvic floor muscles and connective tissues and often presents with pain, urinary incontinence, and reduced quality of life. Although pelvic floor muscle training (PFMT) is commonly used, newer methods such as Hypopressive Exercises (HE) and Pelvic Floor Functional Movement Ret…

NCT07151274 — Impact of Ehlers-Danlos Syndrome on Gynaecological Health

StatusRecruiting
PhaseN/A
SponsorUniversity Hospital, Rouen
Enrollment156
Study TypeOBSERVATIONAL
ConditionsEhlers-Danlos Syndrome (EDS)

Dysmenorrhea is a common problem in gynaecology, significantly impacting patients’ quality of life. Ehlers-Danlos syndrome (EDS) is associated with joint hypermobility, tissue fragility and chronic pain. Some studies suggest an increased prevalence of gynaecological disorders, including dysmenorrhea, in patients with EDS. However, data remain limited and few studies have compared the intensity …

NCT07685847 — Clinical Evaluation of the Efficacy and Safety of a Medical Device in the Form of Rectal Suppositories (Prospidol®) for the Treatment of Symptoms Associated With Chronic Prostatitis/Chronic Pelvic Pain Syndrome.

StatusRecruiting
PhaseN/A
SponsorS&R Farmaceutici S.p.A.
Enrollment40
Study TypeINTERVENTIONAL
ConditionsChronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS)
Interventions

The goal of this clinical trial is to evaluate whether a medical device is effective and safe in treating chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) in adult men.

The main questions it aims to answer are:

  • Does the treatment reduce pain symptoms (measured by NIH-CPSI score) by more than 30% after one month?
  • Does the treatment improve urinary symptoms, quality of life, and s…

NCT07645014 — Comparative Effects of Neurodynamic Stretch and Myofascial Pain Release in Polycystic Ovarian Syndrome.

StatusRecruiting
PhaseN/A
SponsorRiphah International University
Enrollment38
Study TypeINTERVENTIONAL
ConditionsPolycystic Ovarian Syndrome
Interventions;

The study will be a non-blinded randomized controlled trial, consisting of two groups. Non-probability Convenience sampling will be used to recruit participants who will meet the inclusion criteria. Group allocation will be performed using the sealed envelope method to ensure randomization of participants into experimental and control groups. The sample size will be 38 (19 in each group). Group…

NCT07628452 — Comparative Effects of Aerobic Exercises and Jacobson’s Progressive Relaxation Technique in Primary Dysmenorrhea

StatusRecruiting
PhaseN/A
SponsorRiphah International University
Enrollment58
Study TypeINTERVENTIONAL
ConditionsDysmenorrhea
Interventions;

The study will focus on the comparative effects of aerobic exercises and Jacobson’s progressive relaxation technique on pain, fatigue and quality of life in primary dysmenorrhea.

This study will be a randomized clinical trial and will be conducted in, Superior college depalpur and Army public schools and college Lahore (APSACS). Non probability convenience sampling will be used to collect the …

NCT06398990 — The Effect of Cognitive Exercise Therapy Approach and Yoga in Adolescents With Dysmenorrhoea

StatusRecruiting
PhaseN/A
SponsorAcibadem University
Enrollment42
Study TypeINTERVENTIONAL
ConditionsDysmenorrhea; Primary Dysmenorrhea
Interventions; ;

Dysmenorrhoea is a condition that negatively affects the quality of life in women of many age groups. In girls with dysmenorrhoea in adolescence, there is an effect on school performance, self-confidence-depression problems and a decrease in quality of life due to pain. In order to eliminate these negative effects, they should receive a good treatment. Medical treatment usually tries to minimis…

NCT07240883 — ENDO1000 - A UK-wide Endometriosis Research Project

StatusRecruiting
PhaseN/A
SponsorUniversity of Edinburgh
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsEndometriosis
Interventions

Approximately 1.5 million people in the UK, and 200 million globally live with endometriosis, and it is estimated to affect 1 in 10 women of reproductive age. Endometriosis is a chronic pain condition where the lining of the uterus (endometrium) grows in areas outside the uterus. This can cause patients a range of symptoms including severe pain, fatigue, irregular periods, infertility and gastr…

NCT07679074 — CREST: Samphire Guided Care Program on Wellbeing, Work Productivity, and Quality of Life

StatusRecruiting
PhaseN/A
SponsorSamphire Group, Inc.
Enrollment50
Study TypeOBSERVATIONAL
ConditionsPremenstrual Syndrome; Premenstrual Dysphoric Disorder; Dysmenorrhea; Endometriosis; Perimenopause
Interventions;

This study evaluates the feasibility and efficacy of the Samphire Guided Care (SGC) program

  • a 12-week structured digital health program combining clinician-led onboarding, at-home neuromodulation using the Lutea tDCS device, neuromodulation coach support, and app-based symptom tracking - on work productivity, employee wellbeing, and quality of life in individuals experiencing mood and cognit…

NCT07629505 — Oxiblume:CoQ10 (Ralivia) Therapy for Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS)

StatusRecruiting
PhaseN/A
SponsorG.Gennimatas General Hospital
Enrollment100
Study TypeINTERVENTIONAL
ConditionsChronic Pelvic Pain Syndrome (CPPS)
Interventions;

Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS) has a huge socioeconomic impact.Presently, a ‘‘scientific dead-end’’ regarding effective treatment of CP/CPPS is reported. Promising results of clinical studies, regardless their limitations, upon efficacy of phytotherapy for CP/CPPS patients have been published .Phytotherapy is cost effective and avoids the systemic side effects of oth…

Active, Not Recruiting

NCT04333576 — Study Of Oral Elagolix Tablets In Combination With Combined Oral Contraceptive Capsules/Tablets To Assess Dysmenorrhea Response In Adult Female Participants With Endometriosis And Associated Moderate To Severe Pain

StatusActive, not recruiting
PhasePhase 3
SponsorAbbVie
Enrollment800
Study TypeINTERVENTIONAL
ConditionsEndometriosis
Interventions; ;

Endometriosis is a painful disorder of the uterus affecting 6-10% of women of childbearing age. Endometriosis affects daily activities, social relationships, sexuality and sexual activity, and mental health. This study will evaluate how well elagolix in combination with combined oral contraceptives (COC) works within the body and/or how safe it is compared to placebo (does not contain treatment…

NCT07658703 — Physiotherapeutic Approach to Superficial and Deep Dyspareunia in Women With Chronic Pelvic Pain: Comparison Between In-person and Telehealth Care.

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of Sao Paulo
Enrollment72
Study TypeINTERVENTIONAL
ConditionsSurface and Deep Dyspareunia
Interventions;

Adequate sexual function is considered an important factor in satisfaction and overall quality of life for both men and women. It is estimated 16% to 40% of women suffer from some form of sexual dysfunction, which is currently considered a public health problem and its investigation is recommended because it causes significant changes in the quality of life of these women. Among the painful dis…

NCT07544511 — Effect of Hand Massage Stimulation on Pain and Menstrual Symptoms in Primary Dysmenorrhea

StatusActive, not recruiting
PhaseN/A
SponsorInonu University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsDysmenorrhea
Interventions

Purpose of this study: The purpose of this study is to determine the effect of hand massage stimulation techniques on pain, daily menstrual symptoms and nausea and vomiting in primary dysmenorrhea.

H1a: Hand massage stimulation techniques reduce pain in primary dysmenorrhea. H1b: Hand massage stimulation techniques reduce daily menstrual symptoms in primary dysmenorrhea.

The data were collect…

NCT07674433 — Investigation of the Relationship Between Pes Planus and Piriformis Syndrome: A Case-Control Study

StatusActive, not recruiting
PhaseN/A
SponsorKahramanmaras Sutcu Imam University
Enrollment70
Study TypeOBSERVATIONAL
ConditionsPiriformis Syndrome; Pes Planus

The aim of this study is to investigate the relationship between Pes Planus and Piriformis Syndrome. The study will be conducted on individuals aged 18-65 years who are native Turkish speakers, have Turkish reading and writing skills, have been diagnosed with piriformis syndrome, and voluntarily agree to participate. Participants will consist of individuals who have not previously undergone lum…

Not Yet Recruiting

NCT07642271 — Effects of Sahrmann’s Versus Janda Approach in Lower Crossed Syndrome Patients

StatusNot yet recruiting
PhaseN/A
SponsorRiphah International University
Enrollment54
Study TypeINTERVENTIONAL
ConditionsLower Cross Syndrome
Interventions;

Muscular imbalance due to prolonged sitting or standing posture leads to a condition lower cross syndrome(LCS) or lumbopelvic syndrome. Several stretching and strengthening regimens are used to treat cross pattern of muscular tightness and weakness in LCS. This study aims to compare the effects of Sahrmann’s versus Janda’s approach on pain, pelvic tilt and lumbar lordosis in lower crossed syndr…

NCT07652593 — Interaction Between Decidual Cells and NK Cells in Endometriosis

StatusNot yet recruiting
PhaseN/A
SponsorHopital Foch
Enrollment50
Study TypeINTERVENTIONAL
ConditionsEndometriosis
Interventions

Endometriosis is a chronic gynecological disease characterized by the presence of endometrial-like tissue outside the uterus and is frequently associated with pelvic pain and infertility. Increasing evidence suggests that immune dysfunction may contribute to the development and persistence of the disease.

The purpose of this prospective case-control study is to compare immune cell characterist…

NCT07631949 — Osteopathy in Postpartum Lumbopelvic Pain

StatusNot yet recruiting
PhaseN/A
SponsorHalic University
Enrollment45
Study TypeINTERVENTIONAL
ConditionsPostpartum Lumbopelvic Pain; Postpartum Pelvic Girdle Pain; Postpartum Low Back Pain
Interventions; ;

Postpartum lumbopelvic pain is a common condition after childbirth and may affect pain levels, physical function, daily activities, and quality of life.

Conservative treatment options include patient education, exercise, and manual therapy. Although osteopathic manupilative treatment has been shown to improve pain and function in musculoskeletal disorders, limited evidence is available regardi…

NCT07642713 — Effects of MET With and Without Lumbopelvic Manipulation

StatusNot yet recruiting
PhaseN/A
SponsorRiphah International University
Enrollment52
Study TypeINTERVENTIONAL
ConditionsAnterior Pelvic Tilt
Interventions;

The study aims to determine whether lumbopelvic manipulation yields superior improvements in pain, pelvic alignment, and functional ability when combined with METs compared to the treatment provided through METs solely.

NCT07646314 — Comparative Effects of Post-Isometric Relaxation and Reciprocal Inhibition Techniques inPiriformis Syndrome

StatusNot yet recruiting
PhaseN/A
SponsorRiphah International University
Enrollment42
Study TypeINTERVENTIONAL
ConditionsPiriformis Syndrome
Interventions;

Piriformis Syndrome (PS) is a condition which is characterized by pain, numbness, and limited range of motion (ROM) due to compression or irritation of the sciatic nerve by the piriformis muscle. It often leads to discomfort in the buttock region, radiating pain along the posterior thigh, and functional limitations in daily activities. Manual therapy techniques, particularly Muscle Energy Techn…

NCT07661485 — Comparing Two Soft Tissues Technique on Piriformis Syndrome Patients

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of Faisalabad
Enrollment26
Study TypeINTERVENTIONAL
ConditionsPiriformis Syndrome; Musculoskeletal Abnormalities; Sciatica
Interventions;

Piriformis Syndrome is a neuromuscular condition with symptoms of pain, numbness and tingling tracing the route of the sciatic nerve, due to the nerve impingement by the piriformis muscle. Two common manual therapy techniques used to treat musculoskeletal conditions are myofascial release and post-isometric relaxation. The intent of the research is to evaluate the effects of myofascial release …

StatusNot yet recruiting
PhasePhase 2
SponsorCentre Hospitalier Universitaire de Nīmes
Enrollment108
Study TypeINTERVENTIONAL
ConditionsPiriformis Muscle Syndrome
Interventions;

Piriformis muscle syndrome (PMS) is characterized by symptoms caused by compression or irritation of the sciatic nerve by the piriformis muscle as it exits the sciatic notch. PMS commonly evokes the symptoms of sciatica and is likely underdisagnosed. Patients who experience pain related to piriformis syndrome will complain of aggravated pain after prolonged periods of sitting or upon rising fro…

NCT07664956 — Cyclobenzaprine for Postoperative Pain in Minimally Invasive Hysterectomy

StatusNot yet recruiting
PhasePhase 4
SponsorChristiana Care Health Services
Enrollment36
Study TypeINTERVENTIONAL
ConditionsMinimally Invasive Surgical Procedures; Abnormal Uterine Bleeding, Unspecified; Adenomyosis of Uterus; Fibroid Uterus; Chronic Pelvic Pain
Interventions

Typical postoperative pain control after minimally invasive hysterectomy includes ibuprofen, acetaminophen, and a short course of narcotics. The purpose of this study is to see if adding cyclobenzaprine to this regime improves pain control and lessens narcotic use.

NCT07429019 — Intraoperative Bupivacaine Injection to Reduce Acute and Chronic Pain After TVT/TVT-O Surgery. Randomized Double-Blind Trial

StatusNot yet recruiting
PhaseN/A
SponsorHadassah Medical Organization
Enrollment60
Study TypeINTERVENTIONAL
ConditionsPain After Surgery; PSP; Chronic Pain Syndrome; Local Anesthesia Infiltration
Interventions;

This randomized, double-blind controlled trial will evaluate whether intraoperative injection of bupivacaine at the sling insertion site reduces postoperative pelvic and thigh pain in women undergoing TVT or TVT-O surgery for stress urinary incontinence. Women aged 18 years and older scheduled for vaginal surgery including a mid-urethral sling procedure will be randomly assigned to receive eith…

NCT07600697 — Suzetrigine for Opioid-Sparing Postoperative Analgesia Following Transvaginal Pelvic Reconstructive Surgery

StatusNot yet recruiting
PhasePhase 4
SponsorUniversity of California, Los Angeles
Enrollment120
Study TypeINTERVENTIONAL
ConditionsPelvic Organ Prolapse (POP); Stress Urinary Incontinence (SUI); Postoperative Pain
Interventions; ;

Suzetrigine is a selective NaV1.8 inhibitor that provides peripheral analgesia without opioid-related CNS effects. This single-center stepped-wedge randomized clinical trial evaluates whether a suzetrigine-based postoperative analgesic regimen provides non-inferior pain control compared with standard opioid-inclusive care following transvaginal pelvic reconstructive surgery. The study will enro…

NCT07038512 — Evaluation of Hyivy Floora in Managing Interstitial Cystitis/Bladder Pain Syndrome/High-tone Pelvic Floor Dysfunction

StatusNot yet recruiting
PhaseN/A
SponsorWake Forest University Health Sciences
Enrollment10
Study TypeINTERVENTIONAL
ConditionsInterstitial Cystitis/Painful Bladder Syndrome; Interstitial Cystitis, Chronic; High Tone Pelvic Floor Dysfunction
Interventions

The purpose of this study is to test the safety and effectiveness of the Floora Pelvic Rehabilitation Vaginal Dilator in females with Interstitial Cystitis/ Bladder pain Syndrome (IC/BPS) and High-tome Pelvic Floor Dysfunction (HTPFD). After enrollment, participants will be given a Floora device and will be instructed to use the device at least three times per week for 12-weeks in the comfort o…

NCT07645196 — Effects of Physiotherapy on Ultrasound and Clinical Parameters in Women With Dysmenorrhea

StatusNot yet recruiting
PhaseN/A
SponsorVrije Universiteit Brussel
Enrollment80
Study TypeINTERVENTIONAL
ConditionsDysmenorrhea; Endometriosis
Interventions;

Dysmenorrhea affects up to 90% of women of reproductive age and represents a significant public health concern. Beyond prostaglandin-mediated uterine contractions, dysmenorrhea involves central sensitization mechanisms and myofascial components, including abdominal trigger points. Despite growing interest in physiotherapy for chronic pelvic pain, objective data on tissue-level changes induced b…

NCT07605598 — Measuring Pelvic Floor Muscle Fitness Before and After Treatment

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of California, Los Angeles
Enrollment120
Study TypeINTERVENTIONAL
ConditionsMyofacial Pain; Pelvic Pain; Myofascial Pelvic Pain; Chronic Pelvic Pain
Interventions

This study is being done to better understand and improve treatment for myofascial pelvic pain, a common cause of long-lasting pelvic pain in women. Myofascial pelvic pain is related to tight or dysfunctional pelvic floor muscles and can cause pain as well as bladder, bowel, and sexual problems. Current clinical evaluations mostly rely on physical examination and patient-reported symptoms and d…

NCT07659873 — Advancing Online Psychology Tools for Chronic Pain

StatusNot yet recruiting
PhaseN/A
SponsorWomen’s College Hospital
Enrollment60
Study TypeINTERVENTIONAL
ConditionsFibromyalgia; Chronic Pelvic Pain Syndrome
Interventions;

Chronic pain affects more than 20% of Canadians and is associated with significant impacts on physical function, mental health, and quality of life. Despite efforts to improve access to multidisciplinary pain care through centralized referral systems, many patients continue to experience prolonged wait times before receiving treatment.

This study evaluates a self-guided digital psychological i…

NCT07176780 — Effect of Semiconductor Embedded Wearable Sleeve on Treatment of Primary Dysmenorrhea Symptoms

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of California, Davis
Enrollment100
Study TypeINTERVENTIONAL
ConditionsPrimary Dysmenorrhea; Primary Dysmenorrhea (PD); Menstrual Cramps; Women's Health
Interventions;

This study is looking to test a non-compressive semiconductor embedded body sleeve for treatment of primary dysmenorrhea symptoms. Dysmenorrhea is the lower abdominal pain (sometimes referred to as “cramping”) experienced during menstruation (monthly “period”), affecting up to 94% of people aged from 10-20 years old. The semiconductor embedded fabric increases blood circulation through activati…

Enrolling by Invitation

NCT05411549 — The Role of a Mediterranean Diet in Patients With Endometriosis: a Feasibility Trial

StatusEnrolling by invitation
PhaseN/A
SponsorMcMaster University
Enrollment24
Study TypeINTERVENTIONAL
ConditionsEndometriosis
Interventions

This study aims to test if making changes to diet can affect the pelvic pain associated with endometriosis. One group will follow a Mediterranean diet for 12 weeks while the control group will continue with their current diet. We will be looking at the feasibility of a larger-scale trial as well as self-reported quality of life and self-reported pain using standardized questionnaires, that have…

NCT07610044 — Pelvic Floor Exercises Versus Swiss Ball Exercises in Patients With Non-Specific Chronic Low Back Pain

StatusEnrolling by invitation
PhaseN/A
SponsorUniversity of Lahore
Enrollment69
Study TypeINTERVENTIONAL
ConditionsNon-specific Chronic Low Back Pain
Interventions; ;

This randomized controlled trial aims to compare the effectiveness of pelvic floor muscle exercises and swiss ball exercises in females with non-specific chronic low back pain. The study evaluates pain intensity, disability, lumbar range of motion, and core muscle endurance following different rehabilitation protocols.

Completed Trials

NCT00073801 — Pelvic Pain in Women With Endometriosis

StatusCompleted
PhaseN/A
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment78
Study TypeOBSERVATIONAL
ConditionsEndometriosis; Chronic Pelvic Pain

This study will examine pelvic pain associated with endometriosis and explore better approaches to treatment. In women with endometriosis, uterine tissue grows outside the uterus. Standard treatments - altering hormone levels to prevent endometrial tissue growth or surgically removing endometrial tissue - treat pelvic pain only temporarily. This study will investigate the role of sex hormones, …

NCT07633990 — The Effect of vırtual realıty on paın and Sleep qualıty ın Women

StatusCompleted
PhaseN/A
SponsorHasan Kalyoncu University
Enrollment77
Study TypeINTERVENTIONAL
ConditionsDysmenorrhea
Interventions;

The aim of this study is to determine whether a video viewed through virtual reality goggles accompanied by music has an effect on pain and sleep quality in women with dysmenorrhea. The main questions it seeks to answer are as follows:

  • Does watching a video through virtual reality goggles accompanied by music reduce pain in women with dysmenorrhea?
  • Does watching a video through virtual rea…

NCT05570786 — Subdermal Implant-bioabsorbable Gestrinone Pellet for Endometriosis Pelvic Pain Treatment

StatusCompleted
PhasePhase 2
SponsorScience Valley Research Institute
Enrollment100
Study TypeINTERVENTIONAL
ConditionsEndometriosis; Pelvic Pain
Interventions;

Pelvic pain is considered a symptom of multifactorial origin among which Endometriosis is the main gynecological cause affecting 5-10% of worldwide women in their reproductive years, negatively impacting their quality of life and work efficiency. Treatment of endometriosis-associated pelvic pain is challenging and there are surgical and/or hormonal treatments available with variable endpoints. …

NCT07683637 — Effect of Auricular Vagus Nerve Stimulation on Pain and Symptoms in Primary Dysmenorrhea

StatusCompleted
PhaseN/A
SponsorIstanbul Gelisim University
Enrollment40
Study TypeINTERVENTIONAL
ConditionsPrimary Dysmenorrhea (PD); Primary Dysmenorrhea
Interventions;

This study aims to investigate the effects of transcutaneous auricular vagus nerve stimulation (taVNS) on menstrual pain, pain threshold, depression, anxiety, menstrual symptoms, premenstrual syndrome, and functional and emotional impact of dysmenorrhea in young adult women with primary dysmenorrhea.

NCT07680985 — GyneFix IUD Plus LNG-IUS for Adenomyosis

StatusCompleted
PhaseN/A
SponsorWenzhou People’s Hospital
Enrollment270
Study TypeINTERVENTIONAL
ConditionsAdenomyosis
Interventions; ;

Adenomyosis is a common gynecological condition that can cause menstrual pain, heavy menstrual bleeding, anemia, and reduced quality of life. The levonorgestrel-releasing intrauterine system is commonly used as a conservative treatment, but displacement or expulsion of the device may occur, especially in patients with an enlarged uterus or a deep uterine cavity.

This study evaluated whether co…

NCT06112106 — The Effect of Intelligent Exercise and Ergonomic Recommendations on Surgeon Musculoskeletal Discomfort

StatusCompleted
PhaseN/A
SponsorUniversity of Aarhus
Enrollment83
Study TypeINTERVENTIONAL
ConditionsOccupational Injuries; Occupational Exposure
Interventions

The goal of this clinical trial is to investigate the effects of Intelligent Physical Exercise Training (IPET) and ergonomic recommendations on musculoskeletal pain among abdominal and pelvic surgeons. The main question it aims to answer is:

• Is IPET superior to ergonomic recommendations in rehabilitating or preventing musculoskeletal pain?

12 weeks ahead of trial start, all participants wil…

NCT07611331 — Single-Layer Versus Double-Layer Uterine Closure After Primary Cesarean Section

StatusCompleted
PhaseN/A
SponsorHédi Chaker Hospital
Enrollment384
Study TypeINTERVENTIONAL
ConditionsCesarean Scar Defect (Isthmococele); Pelvic Pain; Spotting; Amenorrhea Secondary; Metrorrhagia
Interventions;

This study compares two surgical techniques for closing the uterus after cesarean section: single-layer versus double-layer closure. The primary objective is to determine which technique results in better uterine scar healing, measured by residual myometrial thickness (RMT) and cesarean scar defect (niche) prevalence at 6 weeks and 6 months postoperatively.

BACKGROUND:

Cesarean section is one…

NCT06983600 — The Effect of SuJok Application on Dysmenorrhea and Quality of Life in Young People With Primary Dysmenorrhea:

StatusCompleted
PhaseN/A
SponsorMuş Alparslan University
Enrollment100
Study TypeINTERVENTIONAL
ConditionsDysmenorrhea (Disorder); Alternative Treatment
Interventions

Menarche, which is one of the most prominent features of maturation in adolescents and the transition from childhood to adulthood, causes many problems. The most prominent of these complaints is dysmenorrhea. Primary dysmenorrhea, the most common form of dysmenorrhea, is a gynecological disorder characterized by pain that starts in the lower abdomen before or during menstruation and radiates to…

NCT07458737 — Pelvic Floor Shear-Wave Elastography in Healthy and Pudendal Neuralgia Women

StatusCompleted
PhaseN/A
SponsorComenius University
Enrollment94
Study TypeOBSERVATIONAL
ConditionsPudendal Nerve; Healthy Women
Interventions; ;

This study will compare superficial pelvic floor shear-wave elastography between healthy women and women with pudendal neuralgia.

NCT07062510 — The Effects of Balanced Seating Pressure on Pelvic Asymmetry: A Pilot Study

StatusCompleted
PhaseN/A
SponsorChang Gung Memorial Hospital
Enrollment20
Study TypeINTERVENTIONAL
ConditionsLower Back Pain; Scoliosis Patients
Interventions; ;

The goal of this clinical trial is to learn if the DaSuit® cushion helps reduce discomfort caused by sitting in adults with non-specific low back pain. It will also assess the safety and physical effects of using the DaSuit® cushion. The main questions it aims to answer are:

  1. Does the DaSuit® cushion distribute the pressure evenly on both under-buttock pressure compared to a placebo cushion?…

NCT07052500 — Impact of Seed Cycling on Menstrual Regularity, Dysmenorrhea, and Premenstrual Symptoms

StatusCompleted
PhaseN/A
SponsorLoma Linda University
Enrollment20
Study TypeINTERVENTIONAL
ConditionsMenstruation Disorders; Menstrual Cramps; Menstruation
Interventions

The purpose of this research is to investigate the impact of seed cycling on menstrual regularity, cramps, and pre-menstrual symptoms in women with an irregular menstrual cycle and/or dysmenorrhea. The research seeks to provide evidence-based insights into the potential benefits of seed cycling as a holistic approach to women’s reproductive health.

It is expected that your participation will l…

Other (Terminated)

NCT03281031 — MRI as an Alternative to CT for Exploration of Acute Abdominal Pain in Young Women

StatusTerminated
PhaseN/A
SponsorUniversity Hospital, Montpellier
Enrollment149
Study TypeINTERVENTIONAL
ConditionsAcute Abdominal Pain; Pelvic Pain
Interventions

Objective :

To demonstrate diagnostic performances of Magnetic Resonance Imaging (MRI) as compared to Computed Tomography (CT) as a second intention imaging modality in young women with acute non traumatic abdominopelvic pain and non contributive ultrasonography.

Other (Withdrawn)

NCT05538689 — Surgical Myomectomy Followed by Oral Myfembree Versus Standard of Care Trial (SOUL)

StatusWithdrawn
PhasePhase 4
SponsorUniversity of Chicago
EnrollmentN/A
Study TypeINTERVENTIONAL
ConditionsMetrorrhagia; Pelvic Pain; Menorrhagia; Leiomyoma
Interventions

In this project, the proposition is that the use of daily dosed Myfembree ( a combination of relugolix with estradiol and norethindrone acetate), FDA-approved medication to treat heavy menses fibroid-related symptoms, has the potential to delay the recurrence of fibroid symptoms, prolong the improved quality of life and delay the need for re-intervention after uterine sparing surgery versus the…

NCT05972681 — The PAIN (Pelvic Area Injection for Numbness) Study

StatusTerminated
PhasePhase 4
SponsorMontefiore Medical Center
Enrollment3
Study TypeINTERVENTIONAL
ConditionsVaginal Laceration During Delivery
Interventions; ;

Postpartum pain can interfere with patient’s ability to care for themselves, and their newborn, and untreated pain is associated with risk of greater opioid use, postpartum depression, and development of persistent pain. The research hypothesis of this study is that adding a locally injected analgesic, which will take effect once the epidural analgesia fades, may alleviate perineal pain and imp…