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TRIOMPHE Study

A Multi-arm, Multi-Center, Non-Randomized, Prospective, Clinical Study to Evaluate the Safety and Effectiveness of the NEXUS™ Aortic Arch Stent Graft System in Treating Thoracic Aortic Lesions Involving the Aortic Arch: TRIOMPHE Study

Aortic aneurysm, Aortic stenosis

All genders

18+

Recruiting now

Department of Surgery

Tufts Medical Center

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Collagen Urine Assay

A Novel Urine assay to determine collagen levels in men with severe symptoms of bladder outlet obstruction

Male

50-80

Recruiting now

Department of Urology

Tufts Medical Center

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Treatment Combination of Durvalumab, Tremelimumab and Enfortumab Vedotin or Durvalumab and Enfortumab Vedotin in Patients With Muscle Invasive Bladder Cancer Ineligible to Cisplatin or Who Refuse Cisplatin (VOLGA)

A Phase III Randomized, Open-Label, Multicenter Study to Determine the Efficacy and Safety of Durvalumab in Combination With Tremelimumab and Enfortumab Vedotin or Durvalumab in Combination With Enfortumab Vedotin for Perioperative Treatment in Patients Ineligible for Cisplatin or Who Refuse Cisplatin Undergoing Radical Cystectomy for Muscle Invasive Bladder Cancer (VOLGA)

Bladder cancer

All genders

18+

Recruiting now

Department of Medicine, Cancer Center

Tufts Medical Center

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SUMMIT MAX

A Prospective, Randomized, Controlled, Interventional Clinical Trial to Evaluate the Safety and Effectiveness of the Route 92 Medical MonoPoint® Reperfusion System for Aspiration Embolectomy in Acute Ischemic Stroke Patients

Stroke

All genders

18-85

Recruiting now

Department of Neurosurgery

Tufts Medical Center

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LYS228 Pharmacokinetics for Complicated UTI

A Randomized, Controlled, Evaluator-blinded, Multi-center, study to evaluate LYS228 pharmacokinetics, clinical response, safety and tolerability in patients with complicated urinary tract infection

Urinary tract infections

All genders

18-85

Recruiting now

Department of Urology

Tufts Medical Center

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AbCLO Open Abdomen Study

Assessment of a non-invasive device in the management of Open Abdomen – Pilot Study

Surgery, Trauma

All genders

18-99

Recruiting now

Department of Surgery

Tufts Medical Center

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GORE SYNECOR

Assessment of GORE® SYNECOR Biomaterial in
Focused Patient Populations and Long-Term
Application

Hernia

All genders

18-80

Recruiting now

Department of Surgery

Tufts Medical Center

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Feasibility of a new method for non-invasive monitoring of low-grade bladder cancer

Bladder cancer

All genders

18-90

Recruiting now

Department of Urology

Tufts Medical Center

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Mepi vs. Bupi in Neurosurgery

Mepivacaine versus bupivacaine for neurosurgical procedures

Back pain

All genders

18-99

Recruiting now

Department of Neurosurgery

Tufts Medical Center

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FRED X PAS

MicroVention, Inc. Flow Re-Direction Endoluminal Device X (FRED X) Post-Approval Study

Brain aneurysm

All genders

22-75

Recruiting now

Department of Neurosurgery

Tufts Medical Center

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A Multi-arm, Multi-Center, Non-Randomized, Prospective, Clinical Study to Evaluate the Safety and Effectiveness of the NEXUS™ Aortic Arch Stent Graft System in Treating Thoracic Aortic Lesions Involving the Aortic Arch: TRIOMPHE Study

A Novel Urine assay to determine collagen levels in men with severe symptoms of bladder outlet obstruction

A Prospective, Randomized, Controlled, Interventional Clinical Trial to Evaluate the Safety and Effectiveness of the Route 92 Medical MonoPoint® Reperfusion System for Aspiration Embolectomy in Acute Ischemic Stroke Patients

A Randomized, Controlled, Evaluator-blinded, Multi-center, study to evaluate LYS228 pharmacokinetics, clinical response, safety and tolerability in patients with complicated urinary tract infection

Assessment of a non-invasive device in the management of Open Abdomen – Pilot Study

Assessment of GORE® SYNECOR Biomaterial in
Focused Patient Populations and Long-Term
Application

Feasibility of a new method for non-invasive monitoring of low-grade bladder cancer

Mepivacaine versus bupivacaine for neurosurgical procedures

MicroVention, Inc. Flow Re-Direction Endoluminal Device X (FRED X) Post-Approval Study