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NCT ID: NCT01643746 Withdrawn - Clinical trials for Femoropopliteal Stenosis

Evaluation of Luminal Expansion Following Stenting of Femoro-popliteal Occlusive Disease

Start date: December 1, 2017
Phase: N/A
Study type: Interventional

The primary goal of this trial is to compare prospectively stent opening of Supera (IDEV Technologies) versus a reference stent (LifeStent, Bard Medical) using C-arm CT. A secondary goal is to correlate stent opening with stent patency as documented by Doppler ultrasound at one year post implantation.

NCT ID: NCT01638988 Withdrawn - Insulin Resistance Clinical Trials

Clomifene Citrate Versus Metformin in First-line Treatment of Infertility in Patients With Polycystic Ovary Syndrome and a Resistance to Insulin

Start date: September 2013
Phase: Phase 3
Study type: Interventional

The results of studies conducted until now does not determine what the best way to treat infertility in the first line with patients with Polycystic ovary syndrome (PCOS). This study objective is to determine the best treatment for such patients. The long-term consequence health of women with PCOS are multiple. The woman with PCOS has a risk of developing metabolic diseases, heart diseases, diabetes Type II or anovulatory infertility. The insulin resistance plays an important role in all this medical condition. Clomiphene Citrate (CC) remains the first line treatment to induce ovulation in women with PCOS and anovulatory infertility.

NCT ID: NCT01635543 Withdrawn - Crohn's Disease Clinical Trials

Investigation of Sexual Function in Crohn's Disease Patients With Perianal Fistulas

Start date: October 2011
Phase: N/A
Study type: Observational

Objective: The aim of this study is to investigate whether Crohn's Disease patients with peri-anal fistulas will suffer from sexual dysfunction in an attempt to help us identify Crohn's Disease patients that would benefit from sexual health interventions. Hypothesis: Crohn's patients with active perianal fistulas will have decreased sexual drive, performance, and satisfaction than those with Crohn's Disease in remission.

NCT ID: NCT01625208 Withdrawn - Clinical trials for Peripheral Nerve Block

Supraclavicular Versus Combined Block for Ulnar and Median Distribution Hand Surgery

Start date: March 2012
Phase: N/A
Study type: Interventional

This study will examine how successfully nerves are blocked or frozen for hand surgery. Traditionally, the nerves are frozen at the base of the neck, just above the clavicle or collarbone (the supraclavicular block). This is mostly successful by itself, and provides anesthesia of the entire arm. Occasionally, an additional nerve block is required further down the arm, as the supraclavicular block may have missed a segment, or it is taking too long to come on. In this study the investigators will compare the traditional technique, with a similar but lower volume supraclavicular block plus an immediate low volume block of one nerve further down the arm (the ulnar or median nerve block, depending on which digits are being operated on). The investigators will compare success rates, speed of onset, procedural comfort and length of time of weakness and numbness, plus any adverse events.

NCT ID: NCT01620320 Withdrawn - Stenosis Clinical Trials

Stress Echocardiography Versus Coronary Angiography for Left Main Stenosis Detection

ESTRIE-TC
Start date: July 2010
Phase: N/A
Study type: Observational

Left main stenosis use to be treated by bypass but with the improvement of angioplasty techniques, an increasing number of patients are submit to left main coronary angioplasty. Consequences of left main intra stent stenosis can be disastrous yet, for the moment, no precise recommendation concerning the follow up of these patients exist. The investigators ought to determine if stress echocardiography can predict left main intra stent stenosis as well (non inferiorly)as control angiography that use to be done.

NCT ID: NCT01615692 Withdrawn - Clinical trials for Deep Vein Thrombosis

The 36-month Extension to Follow up Sub Study

Start date: June 2004
Phase:
Study type: Observational

The purpose of this study is to evaluate leg health for one additional year in patients with symptomatic proximal deep venous thrombosis who did not already develop Post-Thrombotic Syndrome (PTS) during the 2 years of follow up in the SOX Trial.

NCT ID: NCT01615627 Withdrawn - Clinical trials for Pulmonary Arterial Hypertension

Hypotonic Treprostinil Subcutaneous Infusion for Control of Treprostinil Related Site Pain

Start date: July 1, 2012
Phase: Phase 4
Study type: Interventional

The investigators will test whether hypotonic (diluted) remodulin solution causes less pain than the eutonic (undiluted) solution supplied by the manufacturer.

NCT ID: NCT01615536 Withdrawn - Rhinosinusitis Clinical Trials

The Role of Canine Fossa Trephination in the Severely Diseased Maxillary Sinus

CFT
Start date: December 2010
Phase: N/A
Study type: Interventional

The hypothesis of this study is that canine fossa trephination (CFT) improves surgical outcomes for patients with a severely diseased maxillary sinus.

NCT ID: NCT01614288 Withdrawn - Clinical trials for Medial Compartment Osteoarthritis of the Knee

High Tibial Osteotomy (HTO) With or Without Arthroscopy of the Knee Joint

Start date: n/a
Phase: N/A
Study type: Interventional

Participants will be randomized to undergo a High Tibial Osteotomy (HTO) with or without a knee scope. Patients will be tested in the Gait Lab, will fill out quality-of-life questionnaires, and have a clinical evaluation done preoperative and at each follow-up visit.

NCT ID: NCT01613924 Withdrawn - Acne Vulgaris Clinical Trials

Efficacy of Handheld Acne Heat Device

Start date: July 2013
Phase: Phase 4
Study type: Interventional

The aim of our study is to determine the time to resolution of individual acne lesions using a popular handheld heat based device in comparison to no treatment and to standard topical therapy with benzoyl peroxide in order to determine its effectiveness in the spot treatment of acne vulgaris. Patient satisfaction and potential side effects will be examined as well.