Clinical Trials Logo

Constriction, Pathologic clinical trials

View clinical trials related to Constriction, Pathologic.

Filter by:

NCT ID: NCT05141604 Recruiting - Hemianopsia Clinical Trials

Feasibility Test of Virtual Reality Obstacle Detection for Low Vision Walking

Start date: May 17, 2022
Phase: N/A
Study type: Interventional

The investigators are developing a new test of pedestrian hazard detection in virtual reality (VR) head-mounted display (HMD) headset, which shows virtual oncoming pedestrians in 3D while subjects are walking in real-world environment, for evaluation of visual field expansion to improve mobility in people with visual field loss.

NCT ID: NCT05140733 Completed - Clinical trials for Lumbar Foraminal Stenosis

Outcomes of Patients With Foraminal Stenosis

Start date: August 22, 2021
Phase:
Study type: Observational

The present study was to see the effect of minimally invasive neural foraminotomy for lumbar foraminal stenosis with unilateral radicular pain. Traditionally, fusion was was done for the patients, but recent development enable surgeon to decompress neural foramen without rigid spinal fusion. Although, clinical effect of neural foraminotomy may have limitation in attaining a comparable result to fusion surgery, a cost-effective analysis may reveal a result in a different perspective. In this regard, we designed a prospective cohort study to see the cost-effectiveness of neural foraminotomy compared to fusion surgery.

NCT ID: NCT05138237 Recruiting - Clinical trials for Indeterminate Common Bile Duct Stricture

Evaluation of (Surgery and Endoscopy) in Management of Indeterminate Common Bile Duct Stricture

Start date: August 1, 2021
Phase: N/A
Study type: Interventional

Evaluate the lower indeterminate CBD strictures trying to reach possible diagnosis by all available methods i.e brush cytology ,bile aspirate cytology , tissue biopsy ,imaging studies and laboratory work up then treatment of the patient either endoscopically or surgically according to the etiology.

NCT ID: NCT05134246 Recruiting - Clinical trials for Radiation-induced Carotid Artery Stenosis

Carotid Revascularization for Radiation Induced Carotid Artery Stenosis

CRICS
Start date: January 5, 2020
Phase:
Study type: Observational [Patient Registry]

Cervical radiotherapy (RT) has greatly reduced the mortality of patients with malignant head and neck tumors, which, however, causes a higher risk of carotid artery stenosis, namely, radiation-induced carotid artery stenosis (RICS) and results in a significant increased risk of ischemic stroke. The systematic review and meta-analysis conducted by our team showed carotid endarterectomy (CEA) can yield better results for these patients than carotid artery stenting (CAS), which was contrary to most previous clinical guidelines. A large-scale prospective study is needed to verify the results. We will conduct a prospective registry of RICS patients treated with CEA to evaluate both short-term safety and long-term efficacy outcomes in a Chinese population.

NCT ID: NCT05133843 Recruiting - Clinical trials for Coronary Artery Stenosis

Complete Functional Assessment of Intermediate Coronary Artery Stenosis Before and After Transcatheter Aortic Valve Implantation (TAVI) in Patients With Severe Symptomatic Aortic Valve Stenosis

CHOICE-FR
Start date: September 29, 2021
Phase: N/A
Study type: Interventional

The purpose of the current study is to assess complete coronary physiology (FFR, RFR, CFR, IMR, and CT-FFR) in TAVI candidates with intermediate coronary artery stenosis before and 6 months after TAVI. This aims to determine how TAVI affects coronary blood flow and coronary microcirculatory function after longer-term follow-up, and how these effects influence FFR and RFR values. In addition, it is aimed to correlate invasive functional testing (FFR and RFR) with non-invasive CT-FFR before and 6 months after TAVI.

NCT ID: NCT05131191 Active, not recruiting - Clinical trials for Coronary Stent Occlusion

CT-FFR for Coronary In-stent Stenosis Based on ISR-Net Algorithm

Start date: January 1, 2022
Phase:
Study type: Observational

CT-FFR(CT-derived flow reserve fraction) usually could not been measured accurately for in-stent lesions due to the serious interference with the metal structs. ISR-Net is a new algorithm in assessing the flow of coronary in-stent stenosis. We compare the CT-FFR value of in-stent lesions with the invasive FFR measured by pressure wire to evaluate the accuracy of ISR-Net algorithm. The research results are of great significance to solve the bottleneck problem of CT-FFR and expand its application scope.

NCT ID: NCT05117515 Enrolling by invitation - Clinical trials for Carotid Artery Stenosis

Retrospective Study of the Uni-Graft® K DV Patch in the Clinical Routine

RESTUGPA
Start date: April 27, 2022
Phase:
Study type: Observational

Uni-Graft® K DV Patch is marketed in Europe since 1999 for reconstructive interventions of the deep femoral, femoral and iliac artery and was also indicated for carotid interventions until 01/2020. Previous studies focused on the clinical performance of different patch materials used for patch angioplasty in different indications, without specifying the product or manufacturer. Thus, it is not surprising that there is a limited amount of published literature available describing the use of the Uni-Graft® K DV Patch in the clinical routine. Therefore, the aim of the present non-interventional study (NIS) is to close this gap by collecting and evaluating existing safety and performance data documented in the clinical routine especially during the application of the Uni-Graft® K DV Patch.

NCT ID: NCT05086016 Active, not recruiting - Clinical trials for Pulmonary Artery Stenosis

Growth Trial: Study of the Renata Minima Stent

Start date: January 14, 2021
Phase: N/A
Study type: Interventional

The objective of the clinical investigation is to access clinical safety and effectiveness of the Minima Stent in neonates, infants, and young children requiring intervention for common congenital vascular stenosis (i.e., coarctation of the aorta and/or pulmonary artery stenosis) who are indicated for treatment.

NCT ID: NCT05078788 Completed - Urethral Stricture Clinical Trials

Holmium Laser Uretherotomy in Combination With Intralesional Steroids in Bulbar Uretheral Stricture

Start date: June 2, 2020
Phase: N/A
Study type: Interventional

the purpose is to evaluate the outcome of visual internal uretherotomy with Holmium laser along with intralesional steroid injection.

NCT ID: NCT05073081 Recruiting - Clinical trials for Lumbar Spinal Stenosis

Feasibility of Prehab for Lumbar Spinal Stenosis

Start date: December 1, 2021
Phase: N/A
Study type: Interventional

The literature has shown evidence of the effectiveness of prehabilitation programs on post-operative recovery for musculoskeletal conditions; however, evidence for prehabilitation for lumbar spinal stenosis (LSS) is limited. Investigators have found that there is very low to low quality evidence for the effect of prehabilitation interventions for improving outcomes following lumbar spine surgery. Therefore, the purpose of this study will be to determine the feasibility of a prehabilitation program for patients undergoing LSS surgery, and pilot test the protocol to provide the foundation for future design of a larger, multicenter randomized controlled trial.