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International Substudy Enigma2 on Postoperative Cognitive Disorders

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
Hali
Wadhamini
University Hospital, Geneva
Washirika
Prince of Wales Hospital, Shatin, Hong Kong
Chinese University of Hong Kong

Maneno muhimu

Kikemikali

The study is a substudy of the Enigma2 trial which aims at investigating the effectiveness and safety of nitrous oxide (N2O) in anaesthesia.The substudy focus is on postoperative cognitive disorders.
Substudy Hypothesis: In patients undergoing anaesthesia for major surgery, administration of N2O will reduce postoperative cognitive disorders when compared with otherwise identically managed surgical patients not receiving N2O as a component of their anaesthesia.

Maelezo

Numerous studies questioned the routine use of nitrous oxide (N2O), the oldest anaesthetic agent used since the development of anaesthesia care. Despite its wide use, there is sufficient doubt as to the risk-benefit profile.

There is strong evidence that N2O is a major risk factor for postoperative nausea and vomiting. It is clear that (even) brief exposure to N2O impairs methionine synthetase, an enzyme required for DNA production, red and white blood cell formation. Tissue hypoxia may be more common. These adverse effects are enhanced in "sick" patients (ie. those at highest risk, with increased hospital length of stay and healthcare expenditure), and will be more likely in longer surgery. At the same time, observational studies and subgroup analysis of published trials suggest that N2O may have beneficial effects in preventing pain and postoperative cognitive disorders

Outcome trial data on postoperative cognitive disorders are lacking in this area for an anaesthetic gas used in more than 90% of all surgery around the world. The enigma2 substudy as a nested study of the large Enigma2 randomised controlled trial aims at answering this question.

The investigators aim at recruiting 420 patients in 2 of the 25 centres participating to the Enigma 2 trials, who are undergoing major surgery.

Tarehe

Imethibitishwa Mwisho: 07/31/2018
Iliyowasilishwa Kwanza: 06/25/2015
Uandikishaji uliokadiriwa Uliwasilishwa: 06/30/2015
Iliyotumwa Kwanza: 07/01/2015
Sasisho la Mwisho Liliwasilishwa: 08/01/2018
Sasisho la Mwisho Lilichapishwa: 08/05/2018
Tarehe halisi ya kuanza kwa masomo: 05/31/2013
Tarehe ya Kukamilisha Msingi iliyokadiriwa: 11/30/2019
Tarehe ya Kukamilisha Utafiti: 05/31/2020

Hali au ugonjwa

Anesthesia
Delirium, Dementia, Amnestic, Cognitive Disorders

Uingiliaji / matibabu

Drug: Nitrous Oxide

Other: Air/Oxygen (placebo)

Awamu

Awamu 4

Vikundi vya Arm

MkonoUingiliaji / matibabu
Active Comparator: Nitrous Oxide
Receives a mixture of 70% Nitrous Oxide in 30% Oxygen
Drug: Nitrous Oxide
Administration of a concentration of 70% Nitrous Oxide with 30% Oxygen in the anaesthetic gas mixture
Placebo Comparator: Air/Oxygen (placebo)
Receives a mixture of 70% Air in 30% Oxygen
Other: Air/Oxygen (placebo)
Administration of a concentration of 70% Air with 30% Oxygen in the anaesthetic gas mixture

Vigezo vya Kustahiki

Zama zinazostahiki Kujifunza 18 Years Kwa 18 Years
Jinsia Inastahiki KujifunzaAll
Hupokea Wajitolea wa AfyaNdio
Vigezo

Inclusion Criteria:

Adult males and females aged ≥ 45 years, undergoing noncardiac surgery and general anaesthesia that exceeds two hours.

At increased risk of cardiac events, defined as any of:

- history of coronary artery disease (angina, MI, Coronary revascularisation-Coronary Artery Bypass Graft (CABG) and Percutaneous Transluminal Coronary Angiography ( PTCA)-, positive stress testing, angiography/other imaging, Q waves on ECG)

- heart failure

- cerebrovascular disease due to atherothrombotic disease

- aortic or peripheral vascular disease

OR

three or more of the following risk factors: age ≥70 years, history of heart failure, diabetes (medicated), hypertension (medicated), preoperative serum creatinine >175 mmol/L, cholesterol ≥6.2 mmol/L, history of a transient ischemic attack (TIA),

Exclusion Criteria:

1. Dementia (MMS test≤24)

2. Parkinson Disease

3. Patients taking regularly (>2 weeks) tricyclic antidepressants or neuroleptics

4. Patients suffering from Alcohol Dependency (WHO CRITERIA )

5. Patients suffering from severe hypoacusis or visual loss or any other reason hindering the CANTAB battery testing process

6. Patients with untreated deficit in Vitamin B6, B12 and folic acid

7. Patients with marked impairment of gas-exchange requiring Fi02> 0.5 intraoperatively

8. Patients with specific circumstances where N2O is contraindicated (eg. volvulus, pulmonary hypertension, raised intracranial pressure) or the use of supplemental oxygen is planned (eg. colorectal surgery)

9. N2O unavailable

Matokeo

Hatua za Matokeo ya Msingi

1. Memory, Executive function, Attention and psychomotor speed using CANTAB Cognitive testing battery [Baseline before surgery]

Validated Computerized testing battery developed by the University of Cambridge for cognitive testing (CANTAB). Patients are tested for baseline cognitive function before surgery

2. Memory, Executive function, Attention and psychomotor speed using CANTAB Cognitive testing battery at 7days following surgery [First assessment (7 days)]

Validated Computerized testing battery developed by the University of Cambridge for cognitive testing (CANTAB). Patients are tested for changes from the baseline cognitive function (before surgery) at 7 days after surgery

3. Memory, Executive function, Attention and psychomotor speed using CANTAB Cognitive testing battery at 3 months following surgery [Second assessment (3 months)]

Validated Computerized testing battery developed by the University of Cambridge for cognitive testing (CANTAB). Patients are tested for changes from the baseline cognitive function (before surgery) at 3 months after surgery

Hatua za Matokeo ya Sekondari

1. ICU stay [up to a maximum of 3 months]

Planned and unplanned admission to the ICU and ICU duration of stay; Follow up to be performed for the whole duration of hospital stay and up to a maximum of 3 months

2. Hospital stay [up to a maximum of 3 months]

Duration of stay in Hospital; Follow up to be performed for the whole duration of hospital stay and up to a maximum of 3 months

3. Quality of life [3 months]

Use of the validated EuroQol test (EQ-5D questionnaire http://www.euroqol.org/)

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