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Hyperplasia clinical trials

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NCT ID: NCT00503581 Terminated - Clinical trials for Stage 0 Uterine Corpus Cancer

Megestrol in Treating Patients With Endometrial Neoplasia or Endometrial Hyperplasia

Start date: July 2007
Phase: Phase 2
Study type: Interventional

This randomized phase II trial is studying how well megestrol works in treating patients with endometrial neoplasia or endometrial hyperplasia. Estrogen can cause the growth of endometrial cancer cells. Hormone therapy using megestrol may fight endometrial cancer by blocking the use of estrogen by the abnormal cells.

NCT ID: NCT00501371 Terminated - Clinical trials for Benign Prostatic Hyperplasia

MCS in Treating Lower Urinary Tract Symptoms (LUTS) Suggestive of Benign Prostatic Hyperplasia

Start date: July 2007
Phase: Phase 3
Study type: Interventional

Phase III, Randomized, double-blind, parallel placebo-controlled study. Two arms: MCS (30mg/day) vs. placebo. Subproject MCS-2: alpha-blocker naïve subjects Subproject MCS-3: subjects responding poorly to alpha-blocker

NCT ID: NCT00497939 Recruiting - Clinical trials for Prostatic Hyperplasia

The Effectiveness of Saw Palmetto and Sanmiaoshan on Benign Prostatic Hyperplasia in Chinese Patients

Start date: January 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the effect of saw palmetto and sanmiaoshan, on top of alpha blocker, on urinary flow rate and BPH symptoms in patients with BPH.

NCT ID: NCT00496639 Recruiting - Stenosis Clinical Trials

Stent vs. Angioplasty for Treatment of Thrombosed AV Grafts: Long-Term Outcomes

Start date: October 2006
Phase: N/A
Study type: Interventional

Arteriovenous grafts are used as the vascular access in 40-50% of hemodialysis patients. Grafts are prone to recurrent stenosis (narrowing) and thrombosis (clotting). Graft clotting is usually due to a narrowing at the site where the graft joins the vein. The standard treatment is to remove the clot and angioplasty the narrowed area. The long-term outcome is not good, lasting only about 1 month. Placing a stent (a small metallic, PTFE covered, spring) at the narrowed site may keep the graft open longer. Principal investigator's preliminary research data suggest that placing a stent at the stenotic site prolongs graft patency following thrombectomy, as compared to conventional angioplasty. This is a single-center, randomized clinical trial, in which patients with a clotted graft with underlying stenosis at the venous anastomosis of the graft will be allocated to thrombectomy + angioplasty (control group) or to thrombectomy + stent placement (study group). The primary endpoint will be primary (unassisted) graft patency. The secondary endpoints will be secondary (assisted) graft patency and overall access-related costs.

NCT ID: NCT00490087 Completed - Clinical trials for Atypical Endometrial Hyperplasia

Resectoscopic Treatment of Atypical Endometrial Polyps in Fertile Women

Start date: January 1999
Phase: Phase 3
Study type: Interventional

The study aims to evaluate the long-term efficacy and prognosis of hysteroscopic resection and coagulation of the base of endometrial polyps with focal atypia in fertile women.

NCT ID: NCT00486785 Completed - Clinical trials for Prostatic Hyperplasia

SAMBA: Sexuality And Management of Benign Prostatic Hyperplasia With Alfuzosin

Start date: April 2006
Phase: Phase 4
Study type: Interventional

Primary Objective: - To assess the sexual function improvement from baseline to the end of treatment (Week 24 or premature withdrawal (PW)) with XATRAL 10mg OD. Secondary Objective: - To evaluate the association between Lower Urinary Tract Symptoms (LUTS) severity and sexual disorders, - To compare the improvement in sexual function, urinary symptoms and Quality of Life among the different regions, - To correlate MSHQ (Male Sexual Health Questionnaire) and IIEF-5 (the 5-Item version of the International Index of Erectile Function), - To assess the onset of action of XATRAL 10mg OD, - To assess the peak flow rate improvement (Qmax), - To assess the safety and the tolerability of XATRAL 10mg OD.

NCT ID: NCT00485186 Withdrawn - Clinical trials for Adrenal Insufficiency

Gene Polymorphisms Influencing Steroid Synthesis and Action

Start date: June 2007
Phase: N/A
Study type: Observational

The extend of steroid biosynthesis and action is mainly dependent on underlying genetic polymorphisms and gene mutations. These sequence variations in multiple genes involved in steroid biosynthesis and action cause different diseases (for example congenital adrenal hyperplasia or disorders of sex development). In addition, sequence variations in several other genes may influence the severity of a genetically caused disease of steroid biosynthesis or action. By this, the differences in an observed phenotype may be explained. Within the study all genes necessary for adrenal and gonadal steroid biosynthesis and several genes which are known to influence the action of steroid hormones will be analysed in patients with congenital disorders of adrenal and gonadal steroid biosynthesis, disorders of steroid action and disorders of sex development. The primary aim is to set up a correlation of the disease phenotype with the different genotypes detected.

NCT ID: NCT00483327 Completed - Clinical trials for Endometrial Carcinoma

Management of Atypical Endometrial Hyperplasia and Endometrial Carcinoma Using Megestrol Acetate

Start date: June 2007
Phase: Phase 2
Study type: Interventional

The purpose of this trial is to study the efficacy, toxicity, and tolerability of a standard hormonal regimen of Megestrol Acetate (Megace) in the treatment of Atypical Endometrial Hyperplasia or well to moderately differentiated endometrial carcinoma.

NCT ID: NCT00472251 Completed - Clinical trials for Benign Prostatic Hyperplasia

One-year Prospective Observational Study of BMI Change Effect of 5-alpha Reductase Inhibitor in Korean BPH Patients

Start date: May 2006
Phase: N/A
Study type: Observational

It is widely-accepted that serum testosterone level and BMI (body mass index) representative of the degree of obesity has negative correlation. Considering the fact that obesity is being mentioned as a risk factor for development of prostate cancer as well as other various life-threatening diseases (example: cardiovascular problems), the effect of BPH treatment agents on BMI is a subject that should certainly be elucidated. Meanwhile, to our knowledge, no prospective study has so far been performed on such issue in Asian population. Prior to generating hypothesis of the effect of 5 alpha reductase inhibitor on BMI, the real effect of 5 alpha reductase inhibitor on BMI change in Korean BPH patients has to be observed in real clinical practice. This study will test the effects of one-year medication of 5 alpha reductase inhibitor on BMI among Korean men with BPH.

NCT ID: NCT00468026 Not yet recruiting - Clinical trials for Benign Prostatic Hyperplasia

Evaluation of the ProstaPlant Prostate Stent Insertion in Ex Vivo Human Prostate

Start date: n/a
Phase: Phase 1
Study type: Interventional

The purpose of this ex-vivo study is to evaluate the insertion procedure for the ProstaPlant implant in human prostates and the support that it supplies to the prostate.