Status: Enrolling
Investigator: Bincy Abraham
Study Coordinator: Beatriz Efron
Phone: 713.363.8890
The purpose of this study is to determine whether RPC1063 is effective in the treatment of Ulcerative Colitis (UC). ... Read more >
Status: Enrolling
Investigator: David Baskin
Study Coordinator: Julie Baskin
Phone: 713.441.3800
The objective of this study is to evaluate the safety and efficacy of FS VH S/D 500 s-apr for use as an adjunct to sutured dural repair in cranial surgery (NCT02891070). ... Read more >
Status: Enrolling
Investigator: Maen Abdelrahim
Study Coordinator: Toniva Boone
Phone: 713.441.0686
This is an open-label, phase 2 comparative study to assess the safety, tolerability, and preliminary efficacy of nal-IRI in combination with other anticancer therapies in patients with advanced pancreatic adenocarcinoma who have not received pri ... Read more >
Status: Open Not Enrolling
Investigator: Richard Klucznik
Study Coordinator: Elmira Ramos
Phone: 713.441.3248
The primary objective of this study is to gather post market data on the Penumbra SMART Coil™ System in the treatment of intracranial aneurysms and other malformations ... Read more >
Status: Enrolling
Investigator: Danielle Antosh
Study Coordinator: Alexandra Villanueva
Phone: 713.441.3879
This randomized, double-blind, placebo-controlled, multi-center, confirmatory study will evaluate the efficacy and safety of Cook MyoSite Incorporated Autologous Muscle Derived Cells for Urinary Sphincter Repair (AMDC-USR) compared to a placebo ... Read more >
Status: Active
Investigator: Rose Khavari
Study Coordinator: Rashmi Pande
Phone: 713.363.9154
The purpose of this study is to provide confirmatory evidence of the safety and efficacy of two Dysport® (AbobotulinumtoxinA) doses (600 units [U] and 800 U), compared to placebo in reducing urinary incontinence (UI) in adult subjects treated fo ... Read more >
Status: Enrolling
Investigator: Charudatta Bavare
Study Coordinator: Kim Donlon
Phone: 713.441.9394
To study the safety and efficacy of drug coated stents for the treatment of venous occlusions and stenoses in the lower extremity. The use of the device for the treatment of peripheral arterial disease is approved by the FDA, however, the use of ... Read more >
Status: Enrolling
Investigator: Jean Bismuth
Study Coordinator: Kim Donlon
Phone: 713.441.9394
This study is a prospective, multicenter, non-randomized single-arm study to assess the feasibility of the treatment of DeBakey Type I/II aortic dissections with the GORE® TAG® Thoracic Branch Endoprosthesis system. ... Read more >
Status: Open Not Enrolling
Investigator: Eric Peden
Study Coordinator: Kim Donlon
Phone: 713.441.9394
This trial will evaluate the safety and efficacy of concentrated bone marrow aspirate (cBMA) to prevent or delay major amputation and/or death in subjects with critical limb ischemia (CLI) due to severe peripheral arterial disease (PAD). ... Read more >
Status: Enrolling
Investigator: Bincy Abraham
Study Coordinator: Beatriz Efron
Phone: 713.363.8890
A Multicenter National Prospective Study of Pregnancy and Neonatal Outcomes in Women with Inflammatory Bowel Disease study is being conducted at the University of California San Francisco and 30 other sites around the United States who are part ... Read more >
Status: Open Not Enrolling
Investigator: Eric Peden
Study Coordinator: Kim Donlon
Phone: 713.441.9394
This research study is designed to assess the safety and effectiveness of an experimental drug called PRT-201 in patients who have chronic kidney disease and who are undergoing surgery to create a new access point to their bloodstream for hemodi ... Read more >
Status: Open Not Enrolling
Investigator: Dale Hamilton
Study Coordinator: Melissa Whipple
Phone: 713.441.3247
UX023-CL303 is a phase 3 multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of KRN23 in adult subjects with XLH. Approximately 120 subjects with a diagnosis of XLH supported by clinical and bioche ... Read more >
Status: Enrolling
Investigator: Colin Barker
Study Coordinator: Amber Jacobs
Phone: 713.441.3905
The purpose of this study is to determine the incidence and predictors of high degree or complete atrioventricular block (AVB) (paroxysmal or persistent) in patients with new-onset persistent left bundle branch block (NOP-LBBB) following transca ... Read more >
Status: Enrolling
Investigator: Joshua Swan
Study Coordinator: Elsie Rizk
Phone: 832.946.0487
Ventilated ICU patients frequently have sepsis and the majority have delirium, a form of brain dysfunction that is an independent predictor of increased risk of dying, length of stay, costs, and prolonged cognitive impairment in survivors. Unive ... Read more >
Status: Open Not Enrolling
Investigator: Dale Hamilton
Study Coordinator: Melissa Whipple
Phone: 713.441.3247
UX023T-CL201 is an, open-label, Phase 2 study. The study will be conducted in adults aged 18 years or older with TIO or ENS whose tumor/skin lesion is inoperable to assess the efficacy and safety of KRN23 administered via subcutaneous injections ... Read more >
Status: Open Not Enrolling
Investigator: Dale Hamilton
Study Coordinator: Melissa Whipple
Phone: 713.441.3247
The primary purpose of this study is to assess the safety and efficacy of repeated subcutaneous (SC) injections of KRN23 in adult subjects with X-Linked Hypophosphatemia (XLH). A Bone Substudy will evaluate the effects of single-blind KRN23 vers ... Read more >
