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Hyperplasia clinical trials

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NCT ID: NCT05460312 Not yet recruiting - Inflammation Clinical Trials

Protein Kinase A in Prostate Cancer Tissue.

Start date: March 1, 2023
Phase:
Study type: Observational

Prostate cancer is the most common malignancy in men. documented risk factors of prostate cancer are age, ethnicity, various genomic mutations and family history of prostate cancer. The cellular mechanisms of malignant transformation are numerous and not completely understood. A possible mechanism is induction of an inflammation resulting in cellular atypia and pre-malignant changes in the affected tissue by inducing a pro-inflammatory response or changes in extra cellular matrix. Protein Kinase A (PKA) is a key stone enzyme in various intra-cellular processes. Various infections' inflammations and malignancies were proved to impact PKA activity. The research hypothesis is that prostate cancer tissue will show a unique profile of PKA activity, regulation and intracellular distribution.

NCT ID: NCT05443451 Recruiting - Clinical trials for Prostate Hyperplasia

BETTY: BEnign Prostatic Hyperplasia Transperineal Targeted Microwave therapY

Start date: September 8, 2022
Phase: N/A
Study type: Interventional

This is a pilot study on applying 3D-Ultrasound-Guided Transperineal Microwave needle ablation for men with symptomatic benign prostatic hyperplasia (BPH).

NCT ID: NCT05440981 Recruiting - Clinical trials for Prostate Hyperplasia

Implanted Nitinol Device (iTind) System in Chinese Males With Lower Urinary Tract Symptom Secondary to BPH

Start date: September 1, 2022
Phase: N/A
Study type: Interventional

This is a prospective series of consecutive cases of patients undergoing iTind for the treatment of male LUTS.

NCT ID: NCT05422833 Completed - Clinical trials for Fibrous Dysplasia of Bone

Effectiveness of Medical Management of Fibrous Dysplasia of Bone.

Efficience
Start date: January 1996
Phase:
Study type: Observational

The objective of our study was to assess the effectiveness of our reference center since its constitution. In a retrospective cohort study, we compared the activity of our center, including the time elapsed between diagnosis and access to the center and the diagnostic delay of patients with fibrous dysplasia between two periods, 1996-2006 (before certification of our center) and 2007-2019 (after certification of our center).

NCT ID: NCT05422677 Completed - Clinical trials for Benign Prostatic Hyperplasia

An Observational Study of Tamsulosin in Patients With Benign Prostatic Hyperplasia

Start date: July 15, 2019
Phase:
Study type: Observational

In this study, BPH patients visited the institutions during the study period and the effectiveness and safety of the treatment of Tamsulosin(Hanmi Tams® Capsule) in real-practice. During the routine medical visit, according to the investigator's judgment, with diagnosis that the Tamsulosin prescription is appropriate, and after deciding to start treatment, patients with BPH who agreed to participate in the study were administered Tamsulosin. As this study is a non-interventional observational study, all subjects received prescriptions according to the routine treatment procedure, and there were no visits or procedures required according to the observational study protocol.

NCT ID: NCT05416606 Completed - Clinical trials for Benign Prostatic Hyperplasia

Prostate Bipolar Enucleation and Resection Versus Open Prostatectomy

Start date: October 1, 2020
Phase: N/A
Study type: Interventional

Benign prostatic hyperplasia (BPH) is a frequent disease in aging men accompanied by bladder outlet obstruction (BOO). Open prostatectomy (OP) is still considered the first-line treatment for more than 80 ml prostate size. In this study, a mixed technique called transurethral bipolar enucleation and resection of the prostate (TBERP) was compared to the standard open prostatectomy.

NCT ID: NCT05415748 Active, not recruiting - Clinical trials for Benign Prostatic Hyperplasia

Deprescribing Tamsulosin in Older Men

PERSONAL
Start date: September 18, 2021
Phase: Phase 4
Study type: Interventional

This is a pilot 12-week randomized, placebo-controlled N-of-1 deprescribing trial among older men receiving chronic tamsulosin therapy for lower urinary tract symptoms attributed to benign prostatic hyperplasia.

NCT ID: NCT05406544 Completed - Fibrous Dysplasia Clinical Trials

Df-Life : Quality of Life in Patients With Fibrous Dysplasia

Df-Life
Start date: November 28, 2022
Phase:
Study type: Observational

Fibrous dysplasia (FD) is a congenital skeletal disorder with multiple complications such as bone pain, fractures, deformities and nerve compression. Few quantitative studies have demonstrated its physical, mental and social negative impacts on patients but none have qualitatively evaluated their global quality of life. Our hypothesis is that a better knowledge of the quality of life of FD patients should allow to target the actions to be implemented to improve patients'care. The main objective of this qualitative research is therefore to investigate the quality of life of FD patients through 2 approaches: a qualitative study with focus groups interviews addressing several themes: self-image, psychological and emotional well-being, difficulties and adaptative strategies; and a quantitative study to measure the impact of FD on quality of life and on olfaction (sometimes affected by nerve compression due to the disease) using standardized questionnaires Short Form 36 (SF36) and Self-reported Mini Olfactory Questionnaire (SELF-MOQ).

NCT ID: NCT05400980 Recruiting - Clinical trials for Benign Prostatic Hyperplasia

The Expander-2 Trial: A Randomized Study to Evaluate the Safety and Efficacy of the Urocross(TM) Expander System and Retrieval Sheath

Start date: July 5, 2022
Phase: N/A
Study type: Interventional

To demonstrate the safety and efficacy of the Urocross Expander System/Retrieval Sheath and the procedure to treat patients with symptomatic Benign Prostatic Hyperplasia (BPH).

NCT ID: NCT05395299 Active, not recruiting - Clinical trials for Prostatic Hyperplasia, Benign

Prostatic Arterial Embolization With SQUID (Ethylene Vinyl Alcohol Copolymer )

SQUID
Start date: November 22, 2022
Phase: N/A
Study type: Interventional

The aim of this pilot study is to analyze the feasibility of prostatic embolization for the treatment of symptomatic benign prostatic hypertrophy with a non adhesive liquid embolic agent (Squid)