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Fistula clinical trials

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NCT ID: NCT03057132 Terminated - Ostomy Clinical Trials

Use of 3M Cavilon Advanced Skin Protectant in the Management of Damaged Skin Around an Ostomy, Drain or Fistula

Start date: November 2016
Phase: N/A
Study type: Interventional

The objective of this pilot study is to evaluate the feasibility, safety and efficacy of 3M™ Cavilon™ Advanced Skin Protectant when used in the management of damaged skin exposed to caustic body fluids from an ostomy, drain site or fistula.

NCT ID: NCT03056664 Not yet recruiting - Crohn's Disease Clinical Trials

The Role of MSC in the Treatment of Fistulas in Patients With Perianal Crohn's Disease

Start date: January 2017
Phase: Phase 2/Phase 3
Study type: Interventional

Here investigators will carry out this phase II clinical trial to explore a effective therapeutic regimen of MSC in the Crohn's perianal fistula.

NCT ID: NCT03055637 Not yet recruiting - Clinical trials for Fistula of Soft Palate (Disorder)

Evaluation of the Incidence of Palatal Fistula in Furlow Double-opposing Z-plasty vs. Two-flap Palatoplasty for Cleft Palate Repair

Start date: February 19, 2017
Phase: N/A
Study type: Interventional

Evaluation of the incidence of palatal fistula in Furlow double-opposing z-plasty versus two-flap palatoplasty for cleft palate repair.

NCT ID: NCT03054623 Recruiting - Clinical trials for Chronic Kidney Diseases

Hemodynamic Assessment of Distal Revascularization Interval Ligation

DRIL
Start date: September 20, 2016
Phase: N/A
Study type: Observational

Our study seeks to define the effect of each component of the distal revascularization interval ligation (DRIL) procedure on the in vivo distal blood pressure of patients with ischemic steal, and to determine whether the interval ligation component of the DRIL procedure is necessary or not.

NCT ID: NCT03044496 Completed - Clinical trials for Arterio-venous Fistula

NIRS Measurement After SCP Block

Start date: September 2016
Phase:
Study type: Observational

Peripheral regional anesthesia induces a sympathectomy-like effect with neurovascular changes causing increased arterial blood flow and venodilatation . Near-infrared spectroscopy (NIRS) can be applied to different kinds of tissue providing oxygen saturation by detecting the absorption and reflection of near-infrared light . The effect on peripheral tissue oxygenation in patients undergoing arteriovenous fistula revision has not yet been examined. We postulate an increase in tissue oxygenation by sympathicolysis caused by peripheral regional anesthesia that might be the reason for beneficial outcome. The aim of our study was to demonstrate the effect of a supraclavicular plexus block in this group of patients.

NCT ID: NCT03041467 Completed - Clinical trials for Arteriovenous Fistula

IN.PACT™ AV Access IDE Study

Start date: April 25, 2017
Phase: N/A
Study type: Interventional

To evaluate the safety and efficacy of the IN.PACT™ AV Access Drug Coated Balloon (DCB) compared to percutaneous transluminal angioplasty (PTA) for treatment of subjects presenting with de novo or non-stented restenotic obstructive lesion of native arteriovenous dialysis fistulae (AVF) in the upper extremity.

NCT ID: NCT03036241 Completed - Clinical trials for Vascular Access Complication

Drug-eluting Balloon vs. Conventional Balloon in the Treatment of (re)Stenosis (Dialysis Fistulae)

DRECOREST2
Start date: January 23, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the use of drug-eluting balloons is effective in the treatment of (re)stenosis in dialysis fistulae.

NCT ID: NCT03029130 Enrolling by invitation - Clinical trials for Vesico Vaginal Fistula

Catheter Extension Trial for Early Vesicovaginal Fistula Repair Failures

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

This study evaluates the use of extending time of continual urinary drainage (using transurethral foley catheter) for patients with early failures of vesicovaginal fistula repairs. Half of those included will be randomized to replacement of foley catheter for a length of 14 additional days, while the other half will be discharged (no intervention). Both groups will be examined for outcomes at 3 months post-repair.

NCT ID: NCT03026491 Completed - Chewing Problem Clinical Trials

Chewing in Children With Repaired Esophageal Atresia-tracheoesophageal Fistula

Start date: January 1, 2017
Phase: N/A
Study type: Observational

The investigators aim to evaluate chewing function in children with repaired esophageal atresia-tracheoesophageal fistula (EA-TEF). Patients with repaired EA-TEF will be evaluated for age, sex, type of atresia. Each child will be required to bite and chew a standardized biscuit. Chewing function will be scored with the Karaduman Chewing Performance Scale (KCPS). The International Dysphagia Diet Standardisation Initiative (IDDSI) will be used to determine the tolerated food texture of children.

NCT ID: NCT03024749 Recruiting - Clinical trials for Spinal Cord Vascular Diseases

Surgical Intervention of Spinal Arteriovenous Malformations and Fistulas

SUIT-SAVM
Start date: December 1, 2016
Phase: N/A
Study type: Observational [Patient Registry]

Spinal arteriovenous fistulas (AVFs) and arteriovenous malformations (AVMs) are complex neurosurgical lesions that are very challenging to manage. Spinal vascular malformations account for 3%-4% of all intradural spinal cord mass lesions. Over the last few decades our understanding of these lesions has dramatically increased thanks to neuroimaging technology (e.g. spinal angiography and indocyanine green angiography). Various treatment modalities including conservative observation, endovascular embolization, microsurgical resection, radiation therapy, and combined therapies have been reported. The treatment for these AVMs and AVFs depends on their location, the type of malformation, the area of the spine involved, and the condition of the patient at the time of treatment. Due to the rarity of these spinal vascular lesions, reports of their management and outcomes have been limited to small series and case reports. And the rates of obliteration and outcomes are not satisfactory, especially the spinal AVMs. Spinal vascular lesions are rare but represent a formidable challenge for the treating neurosurgeon.The purpose of this study is to establish multimodality treatment mode and evaluate the anatomical cure rate and functional preservation rate.