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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02687568
Other study ID # 4439-12
Secondary ID
Status Recruiting
Phase N/A
First received February 16, 2016
Last updated March 5, 2016
Start date May 2014
Est. completion date July 2016

Study information

Verified date February 2016
Source Ruhr University of Bochum
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commitee
Study type Observational

Clinical Trial Summary

Endoscopic examinations and particularly long-lasting interventions can be uncomfortable for patients. Pain and vasovagal reactions are common. Therefore, the implementation is generally recommended under sedation and also carried out in practice here.

The vital signs monitoring to avoid complications is dictated by current national guidelines. Necessary measures of monitoring include pulse oximetry and blood pressure measurements. In patients with severe heart disease an ECG recording should be used additionally. Moreover, the guidelines require that the sedation is clinically monitored continuously to avoid an unwanted anesthetic stage. Such evaluation, however, is often difficult under clinical conditions and even counterproductive, since a constant response and tactile stimulation of the patient (to check clinically the depth level of sedation ), interrupts endoscopic complex intervention. However, clinical most relevant aspect is the avoidance of unrecognized transition of patients from the stage of deep sedation in an anesthetic stage.

Current recommendations do not take into account new study results from a gender perspective, which showed that women and men need a different wake-up time using the EEG derivation means by using the Narcotrend after total intravenous anesthesia, which may be due to different total doses of sedatives needed. However, the research group has been demonstrated in a previous study that most likely caused by the use of EEG monitoring (Narcotrend) an effective adaptation of sedation, in particular a more rapid recovery time by a lower dose of the administered sedative for a continuous sedation stage D0-D2 endoscopic retrograde cholangiopancreatography-(ERCP).

In the presented study the investigators evaluate the extent of gender differences in the wake-up time after sedation with propofol during colonoscopy when using EEG monitoring.


Description:

Endoscopic examinations and particularly long-lasting interventions can be uncomfortable for patients. Pain and vasovagal reactions are common. Therefore, the implementation is generally recommended under sedation and also carried out in practice here.

In interventional and longer lasting interventions (for example colonoscopy, endoscopic ultrasonography, ERCP) as opposed to purely diagnostic examinations is often deep sedation.Use of propofol in terms of sedation efficacy and the wake-up time or quality is superior to the use of benzodiazepines (plus opiates) , while patient safety is the same.

The vital signs monitoring to avoid complications is dictated by current national guidelines. Necessary measures of monitoring include pulse oximetry and blood pressure measurements. In patients with severe heart disease an ECG recording should be used additionally. Moreover, the guidelines require that the sedation is clinically monitored continuously to avoid an unwanted anesthetic stage. Such evaluation, however, is often difficult under clinical conditions and even counterproductive, since a constant response and tactile stimulation of the patient (to check clinically the depth level of sedation ), interrupts endoscopic complex intervention. However, clinical most relevant aspect is the avoidance of unrecognized transition of patients from the stage of deep sedation in an anesthetic stage.

Current recommendations do not take into account new study results from a gender perspective, which showed that women and men need a different wake-up time using the EEG derivation means by using teh Narcotrend after total intravenous anesthesia, which may be due to different total doses of sedatives needed. However, the research group has beendemonstrated in a previous study that most likely caused by the use of EEG monitoring (Narcotrend) an effective adaptation of sedation, in particular a more rapid recovery time by a lower dose of the administered sedative for a continuous sedation stage D0-D2 endoscopic retrograde cholangiopancreatography-(ERCP).

In the presented study investigators evaluate the extent of gender differences in the wake-up time after sedation with propofol during colonoscopy when using EEG monitoring.

Included are patients who undergo diagnostic or therapeutic colonoscopy, which is performed under sedation with propofol.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date July 2016
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age > 18

- Clinical indication for colonoscopy

Exclusion Criteria:

- Lack of consent of the patient

- ASA (American Society of Anesthesiologists) class V

- Known Pregnancy

- Emergency investigations

- Pre-existent hypotension (RRsys <90mmHg), bradycardia (HR <50 / min), hypoxia (SaO2 <90%)

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
EEG monitoring
Value of EEG monitoring as adjunct to standard monitoring

Locations

Country Name City State
Germany Klinikum Agness Karll Laatzen Laatzen

Sponsors (1)

Lead Sponsor Collaborator
Ruhr University of Bochum

Country where clinical trial is conducted

Germany, 

References & Publications (1)

Riphaus A, Wehrmann T, Weber B et al. S3-guidelines-sedation in gastrointestinal endoscopy. Z Gastroenterol. 2008; 46:1298-330. Haensch K, Schultz A, Krauß T et al. Women need more Propofol than men during EEG- monitored total intravenous anaesthesia. Biomed Tech 2009;54: 76- 82 Wehrmann T, Grotkamp J, Stergiou N, Riphaus A et al. Electroencephalogram monitoring facilitates seation with propofol for routine ERCP: a randomized, controlled trial. Gastrointest Endosc (2002); 56: 817- 24

Outcome

Type Measure Description Time frame Safety issue
Primary mean recovery time after propofol sedation for colonoscopy using the EEG recording EEG monitoring at stage D0 to D2 Immediately after the procedure No
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