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Active clinical trials for "Hyperplasia"

Results 611-620 of 926

Safety and Pharmacokinetic Interaction Study of Tadalafil and Dutasteride

Benign Prostate Hyperplasia

This is an open-label, two-arm, one-sequence, cross-over study to evaluate the safety and pharmacokinetic interaction after oral concomitant administration of tadalafil and dutasteride in healthy male volunteers.

Completed2 enrollment criteria

Effects of Chronic Use of Doxazosin in Men With Benign Prostatic Hyperplasia

Benign Prostatic Hyperplasia

In this study, we investigate the changes of the expression of alpha adrenergic receptor in the prostate tissue during 2-yr medication period in the man with benign prostatic hyperplasia. And we also evaluate the efficacy and safety of 24 mo-treatment with doxazosin (4mg, 8mg)

Completed27 enrollment criteria

Safety and Pharmacokinetic Characteristics of DKF-313

Benign Prostate HyperplasiaHealthy

This is a randomized, open-label, single-dose, 2-treatment, 2-way, 2-period crossover study to evaluate the safety and the pharmacokinetic characteristics of DKF-313 (dutasteride and tadalafil) in healthy male volunteers.

Completed30 enrollment criteria

Group-Based Lifestyle Intervention in Measuring Biomarker Levels in Participants at High Risk for...

Atypical Ductal Breast HyperplasiaAtypical Lobular Breast Hyperplasia4 more

This randomized clinical trial studies a group-based lifestyle intervention or usual care in measuring biomarker levels in participants at high risk for breast cancer. Studying the effects that changes to daily eating and exercise habits can have on the body's hormone levels and the body's ability to activate proteins may help doctors identify interventions for individuals at high risk for breast cancer.

Completed22 enrollment criteria

Video Colposcopy in Women With Dysplasia

Uterine Cervical Dysplasia

To assess the effect of live video-colposcopy on women´s anxiety.

Completed8 enrollment criteria

Vaginal Estrogens Comparative Trial on Pelvic Organ Prolapse Patients

Vaginitis AtropicPelvic Organ Prolapse1 more

To evaluate the difference of three vaginal estrogens creams comparative with placebo on improvement of hormonal cytology, local and systemic climacteric complaints, as well as its endometrial security.

Completed8 enrollment criteria

A Randomized, Double-Blinded, Placebo-Controlled, Two-Way Crossover Study to Investigate the Safety...

Prostatic HyperplasiaUrinary Bladder2 more

To investigate the safety and overall tolerability of co-administration two PDE5 inhibitors UK369,003 and sildenafil

Completed5 enrollment criteria

Single Ascending Dose (BMS-813160) Study

Accelerated Intimal Hyperplasia

The primary purpose of this study is to evaluate the safety and tolerability of single oral doses of BMS-813160 in healthy subjects

Completed4 enrollment criteria

Cementation Techniques; an In-vitro Study

Cementation Teeth; HyperplasiaDental Cements1 more

The goal of this observational study invitro study was to compare the different cementation techniques used to lute full veneer crowns on extracted and prepared teeth using Glass Ionomer Cement type 1. The main question[s] it aims to answer are: The in-vitro effect cement application techniques on retention of full veneer crowns. Which of the three different cementation techniques in-vitro provide a greater retention for a full veneer crown and will it achieve better retention using the concluded method for longer duration of cemented crown in oral cavity. To use of adequate amount of cement to avoid wastage. The principal investigator applied the Glass ionomer cement in three different techniques on custom prepared crowns and with the help of an Universal Testing Machine debonded the crown from the prepared tooth. The results were compared amongst the three categories and the technique C, proved to be the superlative amongst the three.

Completed8 enrollment criteria

Pharmacokinetics and Safety/Tolerability of YY-201 in Comparison to Dutasteride and Tadalafil

Benign Prostatic Hyperplasia

A randomized, open label, single dose, two-way crossover clinical trial to investigate the pharmacokinetics and safety/tolerability of YY-201 in comparison to Dutasteride and Tadalafil administered in healthy male volunteers

Completed22 enrollment criteria
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