Építés alatt – nem éles oldal
Belépés
Résztvevőt keres itt: Egyesült Államok4. fázis

Continuous vs Intermittent Ketorolac for Pain Control in Peds CV Surgery

A legfontosabb adatok

Hol
Phoenix (Egyesült Államok)A helyszín megnézése
Fázis
4. fázis

Helyszínek itt: Egyesült Államok

  • Phoenix Children s HospitalPhoenix, Egyesült ÁllamokContact: Kevin Engelhardt, MDRésztvevőt keres

Kérdések a vizsgálat csapatának

  1. Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
  2. Megtérítik az utazási költséget?
  3. Megtarthatom a saját orvosomat?
  4. Mi történik, ha ki akarok lépni?

Contact the study team: see the registry record → Contacts and Locations

Oldal nyomtatása az orvosomnak

A vizsgálat adatai

Ki végzi
Phoenix Children's Hospital
Azonosító
NCT04040452
A regiszteradat frissítve
2026. augusztus 12.
Eredeti leírás
The proposed study will be a prospective, randomized, double blind, placebo controlled trial to compare the use of a continuous infusion versus intermittent ketorolac on postoperative patients in the pediatric cardiovascular ICU. We intend to determine if the continuous infusion leads to a decreased utilization of opiates when compared to intermittent ketorolac.A teljes eredeti leírásKevesebb

Continuous Infusion Versus Intermittent Ketorolac for Postoperative Pain Control in Pediatric Cardiac Surgery Patients

The proposed study will be a prospective, randomized, double blind, placebo controlled trial to compare the use of a continuous infusion versus intermittent ketorolac on postoperative patients in the pediatric cardiovascular ICU. We intend to determine if the continuous infusion leads to a decreased utilization of opiates when compared to intermittent ketorolac.

Bevonási feltételek: All patients aged 3 months to 4 years 11months admitted post operatively to the CVICU during the time period in which the study will be ongoing; Initiation of study medication within the first 12-24 hours post-operatively; The cardiovascular attending of record after review of the intraoperative course and post-operative laboratories determines the patient will receive Ketorolac for pain control.

Kizáró feltételek: Requiring mechanical circulatory support (ECMO) or continuous renal replacement therapy (CRRT) within the first 48 hours post-operatively; History of allergy or sensitivity reaction to ketorolac or any NSAID medications; Orthotopic heart transplantation; Clinically significant bleeding; Patients with known pre-operative medical renal disease, renal transplantation history, congenital or acquired renal abnormality or deformity; Patients that have acute kidney injury, as defined by the letter "I" in the pRIFLE criteria.

ClinicalTrials.gov NCT04040452