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Cysts clinical trials

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NCT ID: NCT03085004 Active, not recruiting - Pancreatic Cyst Clinical Trials

CHARM II: Chemotherapy for Ablation and Resolution of Mucinous Pancreatic Cysts

CHARM
Start date: April 12, 2019
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of chemotherapeutic pancreatic cyst ablation using ethanol lavage followed by the infusion of a dual-agent chemotherapeutic cocktail (paclitaxel + gemcitabine) compared with alcohol-free saline lavage followed by infusion of the same dual-agent chemotherapeutic cocktail (paclitaxel + gemcitabine) for the ablation of pancreatic cystic neoplasms using endoscopic ultrasound guided fine needle infusion (EUS-FNI) for agent delivery.

NCT ID: NCT03066245 Recruiting - Clinical trials for Aneurysmal Bone Cyst

Use of Stem Cells Cultured on a Scaffold for the Treatment of Aneurysmal Bone Cysts (ABC)

Start date: May 3, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

Patients qualified for this study are those diagnosed with ABCs and failed to be treated with other forms of classical therapies. In which, these patients will be engrafted with biodegradable scaffolds seeded with Mesenchymal Stem Cells (MSCs) supplemented with Platelet lysate.

NCT ID: NCT03003013 Recruiting - Clinical trials for Odontogenic Maxillary Cysts

Effect of Biphasic Bone Graft Material With Autologous Platelet-rich Fibrin on Bone Regeneration in a Maxillary Cyst

Start date: November 2016
Phase: Phase 4
Study type: Interventional

Effect of Biphasic Bone Graft Material (BGM) in combination with autologous platelet-rich fibrin (PRF) on bone regeneration in an odontogenic maxillary cyst: a randomized clinical trial

NCT ID: NCT02852447 Completed - Ovarian Cysts Clinical Trials

The Effect of Surgery for Non Endometriosic Ovarian Cysts on Ovarian Reserve

Start date: November 2014
Phase: N/A
Study type: Observational

The main objective is to evaluate the ovarian reserve after laparoscopic cystectomy. The secondary objective is the analysis of predictors of change in the ovarian reserve after surgery

NCT ID: NCT02616757 Withdrawn - Simple Bone Cyst Clinical Trials

Quantitative Ultrasound for the Evaluation of Simple Bone Cyst Healing

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

Simple bone cysts (SBCs), also known as unicameral bone cysts (UBCs), are benign bone lesions. Literature to date describes little agreement between clinicians on specific prognostic criteria for the prediction of cyst healing, recurrence or fracture. Evidence has shown that bone mineral density (BMD) is a reliable indicator of risk to SBC patients given its association with the mechanical properties of bone. There has been further exploration into the use of quantitative ultrasound to assess bone density by measuring the velocity of the ultrasound transmission over the bone. To determine whether the QUS can provide prognostic information with respect to cyst healing, recurrence or fracture with a SBC, further study is needed.

NCT ID: NCT02612740 Completed - Maxillary Cyst Clinical Trials

Deproteinized Bovine Bone in Alveolar Bone Critical Size Defect (>2cm) Secondary to Cyst Removal

Start date: April 2010
Phase: Phase 2
Study type: Interventional

The aim of this study was to evaluate the effect of the use of deproteinized bovine bone as a filler material of critical-sized (diameter >=20 mm) bony defects derived from the excision of maxillary and mandibular cysts. 20 patients were considered. Patients were randomly divided into 2 groups according to the type of treatment: the bone defect was filled with granules of deproteinized bovine bone (test); no filling material (control). Clinical parameters were recorded at 7 days, 1, 6 and 12 months after surgery. Radiological follow up consisted of an orthopantomograph and a CT scan taken at the baseline (pre-operatory) and 12 months after surgery. In order to evaluate the difference in percentage of filling of the bone defect between the two groups, the pre-op and the 1-year radiolucent volumes were evaluated in the CT scans.

NCT ID: NCT02485860 Completed - Pilonidal Cysts Clinical Trials

Interest in the Use of Dressings With Honey for Wound Healing After Excision of Pilonidal Cyst

Pilomiel
Start date: March 8, 2016
Phase: Phase 4
Study type: Interventional

The management of pilonidal cysts is a skin excision and under deep skin. Scarring requires regular dressings (daily for 15 days and then every 48 hours) until complete healing. This healing is obtained on average in 68 days. Some patients have difficulties in healing with a final healing achieved on average in 95 days. Some teams use honey to promote wound cavitary wounds (wound infection, pressure ulcers, varicose wound). The acceleration of wound healing is due to antibacterial properties and hyperosmolarity to reduce secretions. ) The use of honey in pilonidal cysts is not evaluated and may accelerate healing.

NCT ID: NCT02482467 Recruiting - Ovarian Cyst Clinical Trials

Prognosis and Long Term Pubertal Outcome of Girls Previously Diagnosed With a Prenatal Ovarian Cyst

KYSTOV
Start date: November 24, 2014
Phase: N/A
Study type: Interventional

Puberty and long-term ovarian function of patients with a ovarian prenatal cyst has not described to date.

NCT ID: NCT02422147 Recruiting - Pancreatic Cyst Clinical Trials

EUS-guided Ablation of Pancreatic Cyst Neoplasms

Start date: June 1, 2016
Phase:
Study type: Observational [Patient Registry]

This is a registry that will maintain prospective data on the clinical outcomes of all patients with pancreatic cyst lesions who undergo EUS-guided alcohol ablation.

NCT ID: NCT02422095 Withdrawn - Pancreatic Cyst Clinical Trials

Registry of Pancreatic Fluid Collections and Pancreatic Cysts

Start date: February 2015
Phase:
Study type: Observational [Patient Registry]

This registry aims to assess the outcomes of patients undergoing EUS-guided interventions of pancreatic fluid collections and EUS examination of pancreatic cyst lesions.