Swahili
Albanian
Arabic
Armenian
Azerbaijani
Belarusian
Bengali
Bosnian
Catalan
Czech
Danish
Deutsch
Dutch
English
Estonian
Finnish
Français
Greek
Haitian Creole
Hebrew
Hindi
Hungarian
Icelandic
Indonesian
Irish
Italian
Japanese
Korean
Latvian
Lithuanian
Macedonian
Mongolian
Norwegian
Persian
Polish
Portuguese
Romanian
Russian
Serbian
Slovak
Slovenian
Spanish
Swahili
Swedish
Turkish
Ukrainian
Vietnamese
Български
中文(简体)
中文(繁體)

Takotsubo Registry

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
HaliKuajiri
Wadhamini
Cedars-Sinai Medical Center

Maneno muhimu

Kikemikali

The Cedars-Sinai SHI Takotsubo Registry and Proteomic Study is an observational registry that will collect retrospective and prospective demographic, clinical, hemodynamic, laboratory and other diagnostic parameters, therapy and outcome data from individuals who meet the inclusion/exclusion criteria of Takotsubo Registry protocol. Subjects will also be invited to provide a blood sample utilizing a Mitra kit sent to their homes. Researchers from the Barbra Streisand Women's Heart Center will analyze Registry data to identify Takotsubo phenotypes, improve diagnostic capabilities, better predict recurrence rates, and develop targeted Takotsubo treatments.

Maelezo

Registry outreach will begin with an informational and inspirational website and will utilize social media and patient-driven activism through Facebook, blogs and Twitter modalities that have demonstrated efficiencies in other patient-centered research efforts. Subjects will upload specific clinical materials into Cedar-Sinai's web-enabled cloud storage and which will be screened by trained Smidt Heart Institute physicians. The Registry utilizes on-line, e-consent and enrollment connected to a REDCap database that will allow efficient data input for analysis. All potential subjects who have been diagnosed with Takotsubo or have been informed by their physician that they meet diagnosis criteria, will need to provide information for review that includes: hospitalization records, from the time of Takotsubo event, with laboratory data (particularly -- troponin level), ECG and CTA. Registrants will be asked to respond to annual update surveys.

The goal is to accurately understand the prevalence, recurrence and prospective status of the Takotsubo, to determine which individuals are at risk of reoccurrence or subsequent adverse event and to determine potential treatment targets to develop therapeutic strategies

Primary:

- To establish a large USA-based database for patients with Takotsubo with a convenient and easy to use on-line patient-advocate registry using digital media marketing, Box cloud data access and storage, accurate case adjudication, and automated follow-up.

- Participants will also be offered the option of participating in the Takotsubo Proteomic Registry by providing remote ambulatory Mitra blood samples.

Secondary:

• To establish a clinical trial platform for patient-centered point-of-care trials to improve diagnostics, clinical care and outcomes.

Tarehe

Imethibitishwa Mwisho: 03/31/2019
Iliyowasilishwa Kwanza: 03/05/2019
Uandikishaji uliokadiriwa Uliwasilishwa: 04/07/2019
Iliyotumwa Kwanza: 04/09/2019
Sasisho la Mwisho Liliwasilishwa: 04/28/2019
Sasisho la Mwisho Lilichapishwa: 04/30/2019
Tarehe halisi ya kuanza kwa masomo: 01/31/2019
Tarehe ya Kukamilisha Msingi iliyokadiriwa: 01/31/2029
Tarehe ya Kukamilisha Utafiti: 01/31/2029

Hali au ugonjwa

Takotsubo Cardiomyopathy

Awamu

-

Vigezo vya Kustahiki

Zama zinazostahiki Kujifunza 18 Years Kwa 18 Years
Jinsia Inastahiki KujifunzaAll
Njia ya sampuliProbability Sample
Hupokea Wajitolea wa AfyaHapana
Vigezo

Inclusion Criteria:

- Have received a diagnosis of Takotsubo from their physician and consent to enroll

- Submit full medical records needed for Takotsubo adjudication

Exclusion Criteria:

- Younger than 18 years

- Unable to provide informed consent

- Unable to provide the necessary documentation needed for screening purposes

Matokeo

Hatua za Matokeo ya Msingi

1. Number of participants with Prevalence of the Takotsubo [Baseline, Annual follow-up up to 30years]

Prevalence of the Takotsubo will be measured annually. Change from baseline will be assessed.

2. Number of participants with Recurrence the Takotsubo [Baseline, Annual follow-up up to 30years]

Recurrence the Takotsubo will be measured annually. Change from baseline will be assessed.

3. Annual update surveys will collect data on patient's prospective health status following Takotsubo event [Baseline, Annual follow-up up to 30years]

Prospective statusof the Takotsubo will be measured annually. Change from baseline will be assessed.

4. Risk factors affecting which patients, having had one Takotsubo event, will more likely experience a Takotsubo reoccurrence or related subsequent adverse event [Baseline, Annual follow-up up to 30years]

Risk factors for reoccurrence or subsequent adverse event will be collected annually.

Jiunge na ukurasa
wetu wa facebook

Hifadhidata kamili ya mimea ya dawa inayoungwa mkono na sayansi

  • Inafanya kazi katika lugha 55
  • Uponyaji wa mitishamba unaungwa mkono na sayansi
  • Kutambua mimea kwa picha
  • Ramani ya GPS inayoshirikiana
  • Soma machapisho ya kisayansi yanayohusiana na utafutaji wako
  • Tafuta mimea ya dawa na athari zao
  • Panga maslahi yako na fanya tarehe ya utafiti wa habari, majaribio ya kliniki na ruhusu

Andika dalili au ugonjwa na usome juu ya mimea ambayo inaweza kusaidia, chapa mimea na uone magonjwa na dalili ambazo hutumiwa dhidi yake.
* Habari zote zinategemea utafiti wa kisayansi uliochapishwa

Google Play badgeApp Store badge