Clinical Trials Logo

Adenoma clinical trials

View clinical trials related to Adenoma.

Filter by:

NCT ID: NCT02470416 Completed - Polyps Clinical Trials

Prevalence of Small Bowel Polyps in Patients With Sporadic Duodenal Adenomas

SPIDA
Start date: October 2015
Phase: N/A
Study type: Interventional

Little is known about the prevalence of small bowel polyps in patients with sporadic Duodenal/Ampullary polyps. The investigators aim to investigate the prevalence of small bowel polyps in patients with sporadic (ie not related to FAP or PJS) duodenal/ampullary adenomas by performing small bowel capsule endoscopy and comparing the results to those acquired from a control cohort undergoing VCE for accepted indication at our centre.

NCT ID: NCT02468193 Completed - Cushing's Syndrome Clinical Trials

Study of Efficacy and Safety of Osilodrostat in Cushing's Syndrome

Start date: September 24, 2015
Phase: Phase 2
Study type: Interventional

The study aim was to investigate the efficacy and safety of Osilodrostat in patients with Cushing's syndrome due to causes other than Cushing's disease in Japan.

NCT ID: NCT02432599 Completed - Hyperparathyroidism Clinical Trials

Interest of the F18-choline as a Second Line of the Tracer for Detection of Parathyroid Adenomas

APACH1
Start date: March 2015
Phase: Phase 2
Study type: Interventional

The rationale for the proposed pilot study is to investigate the ability of PET-CT with F18-choline to detect and locate the parathyroid adenoma in patients with primary hyperparathyroidism and negative or non-contributory MIBI (Tc-99m sestamibi) and cervical ultrasound, in order to avoid unnecessary bilateral cervical exploration.

NCT ID: NCT02387593 Unknown status - Colorectal Canceer Clinical Trials

Usefulness of Endocuff in the Adenoma Detection Rate. Comparative Study

Start date: September 2014
Phase: N/A
Study type: Interventional

Colorectal cancer (CRC) is one of the leading causes of cancer death worldwide. The cumulative risk of developing CRC is about 6% lifelong. The benefit of screening colonoscopy depends on the detection and removal of all adenomas, however, some of these may be difficult to detect. The "endocuff" (EC) is a polymer sleeve which joins the tip of the colonoscope to improve the image viewing of the mucosa during colonoscopy procedure. There is insufficient evidence of the usefulness of endocuf

NCT ID: NCT02362308 Completed - Clinical trials for Primary Aldosteronism

Glucose Metabolism in Subjects With Aldosterone-Producing Adenomas

Start date: January 2015
Phase:
Study type: Observational

This observational study tests the hypothesis that endogenous aldosterone impairs insulin secretion and insulin sensitivity in subjects with primary aldosteronism.

NCT ID: NCT02357498 Completed - Pituitary Adenoma Clinical Trials

Transsphenoidal Extent of Resection Study

TRANSSPHER
Start date: February 1, 2015
Phase: N/A
Study type: Interventional

The purpose of this research study is to compare the extent of resection (EOR) in patients with nonfunctioning pituitary adenomas undergoing transsphenoidal surgery using a microsurgical technique to those patients who have undergone surgery with a fully endoscopic technique. Another goal is to compare surgical complications, endocrine outcomes, visual outcomes, length of surgery, length of hospital stay, and readmission rates between the two transsphenoidal surgery techniques. This is an observational data collection study with no experimental procedures or experimental medicines. Endonasal transsphenoidal removal of a pituitary tumor is a unique procedure and there is little information comparing the two surgical techniques.

NCT ID: NCT02353533 Recruiting - Adenoma Clinical Trials

Endoscopic Full-thickness REsection of Residual Colorectal Lesions - The FiRE Study

FiRE
Start date: January 2015
Phase: N/A
Study type: Interventional

Adenomatous lesions of the colon are premalignant lesions which have the potential to develop cancer. Therefore adenomas should be resected endoscopically (endo- mucosa resection, EMR). EMR is conducted after submucosal injection of saline which allows to lift the desired lesion prior to resection. In some cases EMR is complicated due to incomplete or failed lifting after the injection of saline. This so- called "non- lifting" sign is a predictor for malignancy of the lesion. Difficult- to- lift polyps are also difficult- to- resect. A higher proportion of these lesions fail to be resected completely using the EMR technique. Alternatively, an over- the- scope full- thickness resection device (FTRD) can be used in order to resect colonic lesions. The FTRD technique has been described elsewhere (Schmidt et al. Gastroenterology 2014; 147: 740-742.e2). No comparative data exists until now on the performance of FTRD resection compared to standard EMR resection of difficult- to- resect colon adenomas. In this study the investigators aim to compare the success of FTRD versus EMR of difficult- to- resect adenomatous lesions (≤ 20 mm).

NCT ID: NCT02332213 Completed - Colorectal Cancer Clinical Trials

Volatile Markers in Digestive Cancer

VOLGACORE
Start date: January 2014
Phase:
Study type: Observational

The study is aimed to determine the potential of volatile marker testing for identification of gastrointestinal cancers (in particular - colorectal and gastric cancers), the related precancerous lesions in the stomach and colon. The study will be addressing the role of confounding factors, including lifestyle factors, diet, smoking as well as addressing the potential role of microbiota in the composition of exhaled volatile markers.

NCT ID: NCT02331836 Completed - Colorectal Polyps Clinical Trials

Endocuff-assisted Versus Cap-assisted Versus Standard Colonoscopy

EC-Cap-SC
Start date: February 2015
Phase: N/A
Study type: Interventional

Comparison of Endocuff-assisted, Cap-assisted and Standard colonoscopy for assessment of the adenoma detection rate (ADR)

NCT ID: NCT02306707 Recruiting - Adenoma, Villous Clinical Trials

Outcomes of Endoscopic Resection of Mucosal and Submucosal Lesions in the Stomach

OERS
Start date: October 2014
Phase:
Study type: Observational

A patient referred to have a lesion in the stomach removed. The aims of this study are to collect information on the technique of endoscopic removal of such lesions. By collecting information on a large number of patients undergoing this procedure the investigators can determine the best ways of diagnosing and removing these lesions safely and effectively.