Trial · NCT01117519
Registered outcomes11
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 11 of 11
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Standard Base Excess | up to 2 days | After administration of 2 litres of study medication. In recovery room. On general ward. |
| Secondary | SID (strong ion difference) | up to 2 days | Change of the SID (strong ion difference) according to the stewart-approach of evalutation acid-base-dysbalances |
| Secondary | Hemodynamic Stability | up to 6 days | Doses and duration of therapy with catecholamins, number and duration of hypotensive episodes |
| Secondary | Fluid Loss of Drainage | up to 6 days | The quantity of fluids per day losing by drainage during the first three days after surgery |
| Secondary | Discharge Criteria, Length of Hospital Stay | 5 days up to hospital discharge | Time until fullfilling the hospital discharge criteria (measured by the postanesthesia discharge scoring system (PADSS)), and length of hospital stay |
| Secondary | Organ Function/Dysfunction | up to 6 days | (Cumulative) frequency of postoperative organ dysfunctions (cerebral, cardiac, pulmonary, renal, gastrointestinal) |
| Secondary | Incidence of Infections | up to 5 days | Perioperative Incidence of infections (according to the Centers of Disease and Prevention (CDC)) |
| Secondary | Pain | up to 6 days | Pain of the patient measured by NAS (Numeric analogue scale), VAS (Visual analogue scale), NRS (Numeric rating scale) and BPS (Behavioral pain scale) |
| Secondary | Incidence of Delirium | up to 6 days | Incidence of delirium measured accordingly by DSM IV (Diagnostic and statistical manual of mental disorders criteria for delirium), Nu-DESC (Nursing delirium screening scale), DDS (Delirium detection score), CAM (Confusion assessment method), CAM-ICU (Confusion assessment method for the ICU), DRS (Delirium rating scale) and ICDSC (Intensive care delirium screening checklist). |
| Secondary | Incidence of Postoperative Cognitive Deficit (POCD) | up to 90 days after surgery | Measurement of cognitive function by 5 tests out of CANTAB (Cambridge neuropsychological test automated battery) modeled by the ISPOCD1 study (International study of post-operative cognitive dysfunction), Stroop colour word test(SCWT) and verbal learning test(VLT) |
| Secondary | Mobilisation | up to 6 days | Duration and type of mobilisation |
Source ClinicalTrials.govtrials-2026-11-12-0.4.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT01117519/registered